CRANIOPLATE Plate Bending Forceps – 120 mm for Cranial Fixation Plates up to 3.0 mm

CRANIOPLATE Plate Bending Forceps, Peak Surgicals SKU PS-000023, are compact reusable neurosurgical instruments designed for controlled bending and contouring of cranial fixation plates before definitive placement. The instrument measures 120 mm / 4 3/4 in overall and is listed by Peak for plates up to 3.0 mm. Its short forceps-style configuration provides direct manual control when small cranial plates require localized adjustment during craniotomy closure, craniofacial reconstruction, skull fixation, or related neurosurgical plating procedures. Rather than relying on powered contouring equipment, the surgeon or operating-room team can make incremental adjustments and repeatedly evaluate plate geometry before fixation. Peak identifies the instrument as CRANIOPLATE branded, reusable, non-sterile, latex-free, and Data Matrix marked. The current listing is priced at $21.99. The exact product name and 120 mm configuration also correspond closely with the Aesculap CRANIOPLATE FM904R device record, although the original manufacturer catalog number should be confirmed from the instrument marking before it is permanently added to the Peak listing.

Compact Forceps Mechanism for Controlled Cranial Plate Contouring

The CRANIOPLATE Plate Bending Forceps use direct manual force through a compact scissors-style or plier-style mechanism to alter the contour of a compatible cranial fixation plate. Once the plate is positioned correctly within the plate-engaging working surfaces, gradual closure of the handles applies localized bending force to the selected area. The 120 mm overall length creates a short, highly controllable instrument profile appropriate for small cranial fixation components where larger orthopedic plate benders would provide unnecessary bulk. Controlled incremental contouring allows the operator to make a small adjustment, release the implant, inspect its shape, and repeat the process only where required. This is particularly important around plate holes and other fixation features because excessive distortion may interfere with screw placement or implant geometry. The bending forceps should engage the plate securely before pressure is applied to reduce slipping or unintended twisting. Repeated aggressive reverse bending should be minimized and all contouring should remain within the limitations specified for the cranial fixation system being used.

Craniotomy Closure and Neurosurgical Fixation Workflow

During craniotomy closure or cranial reconstruction, the CRANIOPLATE Plate Bending Forceps can be used after the bone flap or cranial segment has been repositioned and the surgeon has selected the required fixation plate. If the plate does not follow the intended skull contour closely enough, the implant can be engaged within the bending forceps and adjusted progressively before screw fixation. The short 120 mm configuration provides controlled handling at the sterile field and is appropriate for small fixation plates used around cranial bone. Similar contouring may be required during craniofacial reconstruction or other neurosurgical procedures where a plate must follow a curved osseous surface. Each bend should be followed by reassessment of plate fit rather than attempting to generate the entire contour through one aggressive movement. The plate should also be inspected for damaged holes, excessive twisting, cracks, or prominent tool marks before implantation. Final screw placement and fixation should follow the specific cranial plating system instructions and the surgeon's operative plan.

PS-000023 120 mm Size and Plate Capacity up to 3.0 mm

Peak Surgicals SKU PS-000023 is specifically documented at 120 mm / 4 3/4 in overall with a stated capacity for plates up to 3.0 mm. These specifications should remain attached to this product because cranial and orthopedic plate-bending instruments are produced in substantially different lengths and working capacities. The compact 120 mm format is intended for localized contouring rather than the high leverage required for large-fragment orthopedic plates. Peak also identifies the specialty as neurosurgery and the primary use as bending cranial fixation plates, so PS-000023 should remain positioned around cranial fixation rather than broad long-bone plate contouring. FDA AccessGUDID independently documents an Aesculap CRANIOPLATE Plate Bending Forceps, catalog FM904R, with the exact 120 mm / 4 3/4 in length and reusable non-sterile configuration. Because Peak does not publicly display FM904R, the catalog number and Aesculap manufacturer identity should be confirmed from the Data Matrix or engraving before being added as definitive Shopify specifications.

Reusable Non-Sterile Instrument, Traceability and Procurement Standards

Peak Surgicals identifies the CRANIOPLATE Plate Bending Forceps as reusable, non-sterile, latex-free, and Data Matrix marked. A reusable non-sterile instrument must undergo appropriate cleaning, inspection, and validated sterilization before initial clinical use and after subsequent procedures. Particular attention should be given to the plate-engaging surfaces, pivot area, handle interfaces, and any recessed regions where contamination may accumulate. Following cleaning and rinsing, the forceps should be completely dried and inspected for corrosion, deformation, cracks, excessive joint play, or damaged working surfaces that could affect controlled plate contouring. FDA AccessGUDID identifies the matching CRANIOPLATE FM904R configuration as a reusable prescription surgical forceps supplied non-sterile and lists Aesculap AG as the manufacturer. The GUDID record provides device traceability but should not be described as individual FDA approval. Peak displays CE, FDA, and ISO-related certification badges; institutional purchasers should retain the exact Data Matrix, supplier documents, original manufacturer information where verified, and applicable CE or ISO 13485 procurement documentation.

How do CRANIOPLATE Plate Bending Forceps differ from standard orthopedic Plate Bending Pliers?
CRANIOPLATE Plate Bending Forceps are a compact 120 mm instrument intended specifically for contouring cranial fixation plates in neurosurgical workflows. Standard orthopedic plate bending pliers are often substantially longer and may be intended for thicker small-fragment or long-bone fixation plates. The short CRANIOPLATE configuration provides localized control when working with small cranial implants. Larger orthopedic benders provide greater leverage but may be unnecessarily bulky around cranial fixation systems. Both instruments rely on controlled manual force rather than powered bending. Selection should therefore follow the exact implant system, plate dimensions, anatomical location, and manufacturer-approved contouring technique.

What does the 3.0 mm plate capacity mean for PS-000023?
Peak Surgicals currently states that PS-000023 is suitable for plates up to 3.0 mm. That value should remain tied to this listing rather than being transferred to other CRANIOPLATE or orthopedic bending tools. Cranial fixation plates and meshes are available in multiple geometries, so physical compatibility still needs to be confirmed before bending. A plate should fit securely within the instrument's working surfaces without being forced into the mechanism. The CRANIOPLATE Plate Bending Forceps should only be used within the contouring limits specified for the fixation implant. If a particular plate or mesh requires a different dedicated bending instrument, that system-specific tool should be used instead.

What do the CRANIOPLATE Data Matrix and FDA record mean for procurement?
Peak Surgicals states that the CRANIOPLATE Plate Bending Forceps carry a Data Matrix. FDA AccessGUDID independently lists Aesculap AG model FM904R under the exact CRANIOPLATE Plate Bending Forceps name and 120 mm size. Its Primary DI is 04038653463565 and the database identifies the device as reusable and supplied non-sterile. This provides a strong reference for identifying the original instrument when the Data Matrix or engraving matches. A GUDID record does not mean the individual Peak product should be advertised as FDA approved. Hospitals should retain the physical device identifier, supplier invoice, original manufacturer details, and applicable regulatory documentation for traceability.

How should cranial plates be contoured with the bending forceps?
The plate should first be positioned correctly within the plate-engaging section of the CRANIOPLATE Plate Bending Forceps. The operator should apply a small amount of controlled handle pressure to create an incremental bend. The plate should then be removed or released and its contour reassessed against the required cranial geometry. Additional adjustments can be made gradually until the planned shape is achieved. Excessive bending, repeated reverse bending, and deformation around critical screw holes should be avoided unless specifically permitted by the implant manufacturer. Before implantation, the plate should be checked for appropriate contour, intact fixation holes, absence of cracking, and lack of unintended twisting.

How should hospitals order and reprocess the CRANIOPLATE Plate Bending Forceps?
Hospitals should order the product using Peak Surgicals SKU PS-000023 together with the documented 120 mm length and cranial plate-bending function. Peak currently lists the product at $21.99 and provides a 30-day money-back guarantee on eligible purchases. Because it is supplied non-sterile, the instrument must undergo validated reprocessing before initial clinical use. Staff should inspect the Data Matrix and any manufacturer engraving and record the original catalog number when available. After use, the working surfaces, joint, and handles should be cleaned, rinsed, dried, and inspected for corrosion, deformation, or mechanical damage. Final sterilization should follow the original manufacturer's instructions and the healthcare facility's validated reusable-instrument process before the forceps return to the neurosurgery tray.