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Device Explorer · FDA GUDID · GMDN 38810

Flexible endoscopic biopsy forceps, reusable

A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination. It is typically a flexible metal

US‑registered devices724in commercial distribution
Companies19labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription47%Rx‑only share
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Share of device records

Surgical Direct, Inc.31544%
Sontec Instruments, Inc.13218%
Joimax Gmbh476%
Karl Storz Gmbh & Co. Kg355%
Elmed Incorporated324%
Integra Microfrance324%
American Medical Endoscopy, Inc.314%
Primed Instruments Inc203%

Top labelers

CompanyDevicesShare
Surgical Direct, Inc.31544%
Sontec Instruments, Inc.13218%
Joimax Gmbh476%
Karl Storz Gmbh & Co. Kg355%
Elmed Incorporated324%
Integra Microfrance324%
American Medical Endoscopy, Inc.314%
Primed Instruments Inc203%
Telemed Systems132%
Avalign Technologies, Inc.132%
Richard Wolf Gmbh101%
National Advanced Endoscopy Devices, Inc.101%

Company = labeler of record on GUDID. 19 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NAFlexible biopsy fcps.,oval cup, 5Fr.,400mmFlexible foreign body fcps.,alligator, 7Fr.,400mBIOPSY FORCEPSROTATABLE BIOPSY FORCEPSEndo-KerrisonForcepsSemi-Flexible Biopsy Forceps, up-bitingHandlemahe medical GmbHn.a.MIP Minimal Invasive PCNLOlympusStrauss SurgicalStauss SurgicalAED

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

FDA product codes

CodeNameDevices
FCLFORCEPS, BIOPSY, NON-ELECTRIC179
GCJLaparoscope, general & plastic surgery141
KAEFORCEPS, ENT92
EOQBRONCHOSCOPE (FLEXIBLE OR RIGID)44
LRYPUNCH, SURGICAL43
GENFORCEPS, GENERAL & PLASTIC SURGERY34

GMDN & GCC registration

  • GMDN code 38810 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 47% · 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 (Inch) · 133Length (Millimeter) · 16Outer Diameter (Millimeter) · 16Length (Centimeter) · 2

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

How many flexible endoscopic biopsy forceps, reusable products are registered in the US?

724 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Flexible endoscopic biopsy forceps, reusable", from 19 companies. The largest labeler is Surgical Direct, Inc. with 44% of records.

Which FDA product codes apply?

FCL (FORCEPS, BIOPSY, NON-ELECTRIC), GCJ (Laparoscope, general & plastic surgery), KAE (FORCEPS, ENT), EOQ (BRONCHOSCOPE (FLEXIBLE OR RIGID))

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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