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Root Forceps, SKU PS-OT-0498, is a dental extracting instrument manufactured from German stainless steel for controlled engagement of retained roots, mandibular anterior teeth, and premolar roots during exodontia. The available pattern is PS-6902 No. 151A, with an angled beak profile designed for apical purchase after periodontal ligament expansion and elevator-assisted luxation. Its opposing beaks adapt around the root surface at the cervical and subgingival levels, while the pivoted handle transfers hand pressure into controlled buccolingual movement. This instrument is used in simple dental extraction, retained root removal, root tip delivery after crown fracture, premolar extraction, pre-prosthetic clearance, and surgical extraction following flap reflection when the root segment has been mobilized. It supports oral and maxillofacial surgeons, dental surgeons, periodontists, dental clinics, hospital dental departments, ambulatory oral surgery units, and procurement teams maintaining reusable extraction trays for routine and surgical dental procedures.
The No. 151A pattern works through a pivoted extraction mechanism that converts handle compression into opposing beak closure at the working end. The angled beaks allow the operator to approach mandibular anterior and premolar roots without excessive handle interference against the opposing arch. The slim terminal profile seats along the root surface after luxation, creating apical purchase before rotational or buccolingual delivery force is applied. The joint maintains alignment between the handles and the paired working tips, keeping the gripping axis stable as pressure increases. The textured handle surface improves instrument control when gloves are wet during irrigation, flap management, or socket debridement. The rounded handle ends reduce localized palm pressure during repeated extractions. The beak curvature supports engagement below the cemento-enamel region or along exposed root structure, while the proximal head geometry provides leverage close to the alveolar crest. This design is suited to controlled root delivery rather than broad crown grasping, making it appropriate when remaining tooth structure is reduced.
During dental extraction, this instrument is introduced after clinical assessment, periodontal ligament release, and elevator mobilization. In a non-restorable mandibular incisor or premolar, the beaks are positioned at the cervical root surface after gingival cuff separation, then advanced apically as socket expansion permits. For retained root removal, the operator first creates mobility with a straight elevator, Coupland elevator, or luxator, then applies the No. 151A pattern to secure the exposed segment without crushing the surrounding alveolar plate. In surgical extraction, the forceps can be used after mucoperiosteal flap reflection and bone removal when the root has been sectioned or loosened. The working end supports buccolingual movement, rotational control on compatible single-rooted teeth, and final delivery once resistance has been reduced. Dental surgeons use it in outpatient oral surgery, emergency dentistry, periodontal extraction planning, and pre-prosthetic clearance. Procurement teams can place it in routine extraction cassettes for clinics that require a narrow-beak instrument for root-focused dental workflows.
The PS-6902 No. 151A variant is selected when the clinical target is a reduced coronal structure, retained root, or mandibular anterior-to-premolar extraction case requiring narrow beak access. Its beak angulation helps the operator maintain a favorable line of approach while keeping the handles clear of the lip, cheek, and opposing dentition. For mandibular incisors, the narrower profile permits placement close to the root surface after circumferential ligament release. For lower premolars, the same geometry provides controlled grasping when the crown is fractured, heavily restored, or prepared for sectioned removal. In root tip procedures, the instrument is used after the fragment is exposed and loosened, not as the first instrument for deeply embedded apical fragments. Compared with broader universal extraction patterns, this design is more focused on root purchase and access in restricted anterior or premolar zones. It fits extraction setups that also include elevators, periosteal elevators, curettes, suction, and socket irrigation instruments for complete exodontic workflow.
German stainless steel provides the rigidity required for repetitive compression, controlled leverage, and resistance to deformation at the beaks and joint. The listed satin, dull, and mirror finish options support different handling preferences in dental operatories and central sterile supply departments. A satin or dull surface reduces reflective glare under chairside lighting, while a mirror finish allows fast visual inspection during cleaning. The reusable design supports steam autoclave processing after thorough manual cleaning, ultrasonic cleaning where used by the facility, drying, inspection of the joint, and packaging in extraction cassettes. CE marking and ISO 13485 certification align the instrument with documented quality management and regulated procurement expectations for hospitals, clinics, distributors, and dental supply teams. FDA procurement context supports purchasing documentation for international healthcare markets requiring traceability and compliance records. The Class I classification, one-year warranty, OEM availability, MOQ of one piece, and return or replacement after-sale support make the product suitable for single-clinic ordering and distributor replenishment.
| SKU | PS-OT-0498 |
|---|---|
| Product Name | Root Forceps |
| Price | $6.05 |
| Size/Gauge Variants | PS-6902 No. 151A |
| Instrument Category | Dental Extracting Forceps |
| Procedure | Dental extraction, retained root removal, mandibular anterior extraction, premolar extraction, surgical exodontia |
| Material | German Stainless Steel |
| Finish | Satin, dull, mirror |
| Sterilization | Reusable and autoclavable after standard instrument cleaning |
| Instrument Classification | Class I |
| Reusable | Yes |
| Certifications | CE, ISO 13485, FDA |
| Warranty | 1 year |
| MOQ | 1 piece |
| OEM / Custom Orders | Available |
| After-Sale Service | Return and replacement support |
How does Root Forceps differ from standard No. 150 universal extraction forceps?
Root Forceps in the No. 151A pattern is selected for mandibular anterior teeth, premolars, and retained root segments where narrower beak access is required. A No. 150 universal extraction forceps is commonly used for maxillary anterior and premolar extraction, with a different working angle for the upper arch. The No. 151A pattern provides lower-arch access and root-focused beak geometry rather than a broad crown-grasping profile. Its angled head helps the operator approach the cervical root surface while keeping the handles clear during mandibular extraction. The difference is clinically important when crown structure is fractured or insufficient for standard engagement. Root Forceps is therefore placed in extraction trays where retained root delivery and lower premolar exodontia are routine.
When is the PS-6902 No. 151A pattern selected during dental extraction?
The PS-6902 No. 151A pattern is selected for mandibular incisors, lower premolars, and accessible retained roots after adequate luxation. In an anterior extraction, the beaks are placed close to the root surface after periodontal ligament release. In a lower premolar case, the instrument is used when mobility has been created and the operator needs controlled buccolingual delivery. For a fractured crown, it is used after the remaining root has been exposed enough for secure beak placement. Root Forceps is not intended to replace elevators, because apical seating depends on prior mobilization. This selection keeps extraction force focused on the root rather than unsupported coronal fragments.
How do CE, ISO 13485, and FDA documentation support procurement?
CE marking supports regulated purchasing documentation for healthcare buyers requiring product conformity records. ISO 13485 indicates that the manufacturing quality system is structured for medical device production and traceability. FDA documentation supports procurement teams that need compliance files for regulated medical supply channels. Hospitals, clinics, and distributors use these records during vendor review, product onboarding, and repeat ordering. Root Forceps can therefore be listed in purchasing systems with recognized device documentation. The same documentation is useful for international buyers comparing extraction instruments across dental supply tenders.
How is the pivot mechanism used intraoperatively?
The pivot mechanism aligns the two handles with the opposing beaks and allows controlled closure around the root surface. During use, the operator seats the beaks apically, then compresses the handles until the working tips grip the target structure. The joint keeps the closing path stable, reducing uncontrolled tip displacement during buccolingual movement. After mobility is confirmed, the clinician applies measured delivery force through the handles rather than excessive squeezing. Root Forceps depends on this pivot action for controlled purchase during retained root removal. The textured grip supports hand stability while the joint transfers pressure to the working end.
What should hospitals and clinics know about sterilization and ordering?
This instrument is reusable and compatible with standard dental instrument reprocessing workflows. Cleaning removes blood, tissue, cement, and debris from the beaks, hinge area, and handle texture before sterilization. The joint is opened during cleaning and inspected for movement before packaging. Steam autoclave processing follows the facility’s approved cleaning and drying sequence. Root Forceps is supplied with a one-year warranty, MOQ of one piece, OEM availability, and return or replacement after-sale support. These terms make it suitable for clinic-level replacement orders, hospital dental trays, and distributor stock replenishment.
Order Processing: We strive to serve you promptly! Orders placed before the cut-off time of 5:00 PM (GMT -05:00) (Eastern Standard Time) will be processed the same business day. Orders placed after this time will be processed the next business day.
Handling Time: Our standard handling time is 1-2 business days (Monday through Friday). This includes order verification, quality checks, packaging, and dispatch. Please note that orders placed on weekends or holidays will be processed on the following business day.
Transit Time: Once dispatched, the estimated transit time is 4-5 business days (Monday through Friday). However, transit times may vary depending on your location and any unforeseen circumstances.
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We proudly offer worldwide shipping, ensuring that our premium surgical instruments are accessible to healthcare professionals across the globe. No matter where you are, you can count on us to deliver quality tools right to your doorstep!
To provide you with confidence in your purchase, we offer a 1-year warranty as well as a 30-day money-back guarantee on all non-personalized orders.
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At Peak Surgicals, customer satisfaction and product quality are important to us. We offer a straightforward 30-day return policy, allowing eligible items to be returned within 30 days of delivery.
To qualify for a return, the item must be unused, in its original condition, and returned in the original packaging with tags, labels, and proof of purchase included.
Items must not show signs of use, alteration, damage, sterilization, or clinical handling after delivery.
To start a return, please contact us at info@peaksurgicals.com with your order number, product details, and reason for return.
Approved returns should be sent to:
Peak Surgicals
364 E Main Street
Middletown, DE 19709
Delaware, United States
No Restocking Fee: We do not charge restocking fees on approved returns.
Free Returns: If the item is incorrect, defective, or damaged during shipping, Peak Surgicals will cover the return shipping cost.
Customer Responsibility: If the customer ordered the wrong item or no longer needs the product, the customer is responsible for the return shipping cost.
Returned products must be received in new, unused condition with all labels, packaging, and documentation intact. Items that are used, damaged, altered, incomplete, or returned without approval may not be eligible for a refund.
Once your return is received and inspected, we will notify you whether the refund has been approved. Approved refunds will be processed to the original payment method within 10 business days.
Please note that your bank or credit card provider may require additional time to post the refund to your account.
Please inspect your order immediately after delivery. If your item is defective, damaged, or incorrect, contact us at info@peaksurgicals.com as soon as possible with your order number and clear photos of the product and packaging.
Certain items may not be eligible for return, including customized products, personalized instruments, special-order items, clearance items, sale items, and gift cards.
For exchanges, please return the original item after approval and place a new order for the replacement item. This helps ensure faster processing and accurate product selection.
Peak Surgicals supplies surgical, dental, orthopedic, gynecology, and veterinary instruments to healthcare professionals, clinics, hospitals, distributors, and procurement buyers worldwide.
For orders shipped to the European Union, customers may have the right to cancel or return an eligible order within 14 days of receipt, provided the item is unused, in its original condition, and returned with all original packaging and proof of purchase.
For return, refund, or exchange inquiries, please contact us:
Phone: +1 315 526 9968
Email: info@peaksurgicals.com