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Device Explorer · FDA GUDID · GMDN 46688

Bone cutting forceps, reusable

A strongly constructed, hand-held, surgical instrument used for cutting posterior rib ends and bone tissue during a surgical procedure. It typically has very strong, sharp, angled cutting blades attached to strong, sprung (self-opening), pivoted or multi-pivot

US‑registered devices641in commercial distribution
Companies45labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription69%Rx‑only share
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Share of device records

Integra Lifesciences Production Corporation518%
Mizuho Corporation427%
Sklar Corporation396%
Helmut Zepf Medizintechnik Gmbh386%
Rz-Medizintechnik Gmbh345%
Avalign Technologies, Inc.345%
Hayden Medical, Inc.325%
Richard Wolf Gmbh315%

Top labelers

CompanyDevicesShare
Integra Lifesciences Production Corporation518%
Mizuho Corporation427%
Sklar Corporation396%
Helmut Zepf Medizintechnik Gmbh386%
Rz-Medizintechnik Gmbh345%
Avalign Technologies, Inc.345%
Hayden Medical, Inc.325%
Richard Wolf Gmbh315%
Teleflex Incorporated284%
Gimmi Gmbh264%
Gsource Llc264%
Evonos Gmbh & Co. Kg244%

Company = labeler of record on GUDID. 45 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NASurgicalTri-D Kerrison RongeurKerrison rongeurMicro-RongeurKerrison Rongeur 180 x 1 mm, 35 deg, UpwardKerrison Rongeur 180 x 5 mm, 35 deg, UpwardKerrison Rongeur 180 x 4 mm, 35 deg, UpwardKerrison Rongeur 180 x 3 mm, 35 deg, UpwardKerrison Rongeur 150 x 5 mm, 35 deg, UpwardKerrison Rongeur 150 x 4 mm, 35 deg, UpwardKerrison Rongeur 150 x 3 mm, 35 deg, UpwardKerrison Rongeur 150 x 2 mm, 35 deg, UpwardBMT Medizintechnik GmbHFENTEXSCHWERT

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
HTZINSTRUMENT, CUTTING, ORTHOPEDIC141
EMHFORCEPS, RONGEUR, SURGICAL72
GENFORCEPS, GENERAL & PLASTIC SURGERY40
KBBRongeur, Nasal39
EMHForceps, Rongeur, Surgical38
NBHAccessories, arthroscopic33

GMDN & GCC registration

  • GMDN code 46688 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 69% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 75Length (Centimeter) · 28Length (Inch) · 28Outer Diameter (Millimeter) · 25Width (Millimeter) · 6

Use these as the dimensions to specify in a tender line.

How many bone cutting forceps, reusable products are registered in the US?

641 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone cutting forceps, reusable", from 45 companies. The largest labeler is Integra Lifesciences Production Corporation with 8% of records.

Which FDA product codes apply?

HTZ (INSTRUMENT, CUTTING, ORTHOPEDIC), EMH (FORCEPS, RONGEUR, SURGICAL), GEN (FORCEPS, GENERAL & PLASTIC SURGERY), KBB (Rongeur, Nasal)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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