A rigid, hand-held manual surgical instrument designed to be introduced through the working channel of an endoscope and/or an endoscopic port (e.g., laparoscopic port) primarily for grasping and manipulating tissues during endoscopic surgery. It has proximal c
| Company | Devices | Share |
|---|---|---|
| National Advanced Endoscopy Devices, Inc. | 5,867 | 38% |
| Elmed Incorporated | 1,685 | 11% |
| Novo Surgical, Inc. | 1,311 | 8% |
| Avalign Technologies, Inc. | 1,195 | 8% |
| Endoplus | 909 | 6% |
| Sopro-Comeg Gmbh | 595 | 4% |
| Karl Storz Gmbh & Co. Kg | 504 | 3% |
| Ambler Surgical Corp. | 446 | 3% |
| Flexbar Machine Corporation | 411 | 3% |
| Steris Corporation | 295 | 2% |
| Integra Microfrance | 285 | 2% |
| Scanlan International Inc | 234 | 2% |
Company = labeler of record on GUDID. 50 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 5,985 |
| GCJ | Laparoscope, general & plastic surgery | 3,514 |
| GCJ | Laparoscope, General & Plastic Surgery | 3,172 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 2,217 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1,984 |
| HET | Laparoscope, Gynecologic (And Accessories) | 698 |
Use these as the dimensions to specify in a tender line.
15,492 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid endoscopic tissue manipulation forceps, reusable", from 50 companies. The largest labeler is National Advanced Endoscopy Devices, Inc. with 38% of records.
GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GCJ (Laparoscope, general & plastic surgery), GCJ (Laparoscope, General & Plastic Surgery), GEI (Electrosurgical, cutting & coagulation & accessories)
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.