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Device Explorer · FDA GUDID · GMDN 38661

Rigid endoscopic grasping forceps, reusable

A rigid hand-held, manual device used in combination with a compatible endoscope to grasp tissue (typically atraumatically) or foreign bodies. It is typically constructed as a very long instrument with one sliding and one stationary rod whose distal ends are e

US‑registered devices141in commercial distribution
Companies11labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription76%Rx‑only share
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Share of device records

Smith & Nephew, Inc.5438%
Sopro-Comeg Gmbh2014%
Avalign Technologies, Inc.1913%
Karl Storz Gmbh & Co. Kg1813%
Gsource Llc86%
National Advanced Endoscopy Devices, Inc.75%
Steris Corporation54%
Mahe Medical Gmbh43%

Top labelers

CompanyDevicesShare
Smith & Nephew, Inc.5438%
Sopro-Comeg Gmbh2014%
Avalign Technologies, Inc.1913%
Karl Storz Gmbh & Co. Kg1813%
Gsource Llc86%
National Advanced Endoscopy Devices, Inc.75%
Steris Corporation54%
Mahe Medical Gmbh43%
Hermann Medizintechnik Gmbh32%
Olympus Winter & Ibe Gmbh21%
Sklar Corporation11%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Foreign body fcps.,alligator 5Fr.,400mm, semi-riEndoclinch grasp.fcps.insert,fenestrated d/a, 5/Hermann Medizintechnik GmbHCystoscopy instrumentArthroscopy hand instrumentsGrasping forcepsmahe medical GmbHCardioFITn.a.OlympusARTHRO-PIERCENAACUFEXACUFEX / PITBULLEndoEndo-Hips

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

FDA product codes

CodeNameDevices
NBHACCESSORIES,ARTHROSCOPIC43
FBMCannula and trocar, suprapubic, non-disposable30
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES24
HRXARTHROSCOPE18
GCJLaparoscope, general & plastic surgery16
GEIElectrosurgical, Cutting & Coagulation & Accessories8

GMDN & GCC registration

  • GMDN code 38661 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 76% · 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

Width (Millimeter) · 9Length (Centimeter) · 8Length (Inch) · 1

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

How many rigid endoscopic grasping forceps, reusable products are registered in the US?

141 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid endoscopic grasping forceps, reusable", from 11 companies. The largest labeler is Smith & Nephew, Inc. with 38% of records.

Which FDA product codes apply?

NBH (ACCESSORIES,ARTHROSCOPIC), FBM (Cannula and trocar, suprapubic, non-disposable), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), HRX (ARTHROSCOPE)

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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