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
| Company | Devices | Share |
|---|---|---|
| Ningbo Xinwell Medical Technology Co., Ltd. | 384 | 18% |
| Hangzhou Ags Medtech Co., Ltd. | 384 | 18% |
| Beijing Zksk Technology Co.,Ltd | 349 | 17% |
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | 224 | 11% |
| Endoch Inc | 163 | 8% |
| Micro-Tech (Nanjing) Co., Ltd. | 123 | 6% |
| Cook Incorporated | 89 | 4% |
| Olympus Medical Systems Corp. | 85 | 4% |
| Taewoongmedical.Co.,Ltd | 56 | 3% |
| Primed Instruments Inc | 26 | 1% |
| Caelaris Medtech, Inc. | 23 | 1% |
| Alton (Shanghai) Medical Instruments Co., Ltd. | 21 | 1% |
Company = labeler of record on GUDID. 35 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 |
|---|---|---|
| FCL | Forceps, Biopsy, Non-Electric | 1,950 |
| HFB | Forceps, Biopsy, Gynecological | 164 |
| PTS | Endoscopic grasping/cutting instrument, non-powered, exempt | 90 |
| FCL | FORCEPS, BIOPSY, NON-ELECTRIC | 79 |
| KNW | INSTRUMENT, BIOPSY | 20 |
| KGE | FORCEPS, BIOPSY, ELECTRIC | 13 |
Use these as the dimensions to specify in a tender line.
2,098 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Flexible endoscopic biopsy forceps, single-use", from 35 companies. The largest labeler is Ningbo Xinwell Medical Technology Co., Ltd. with 18% of records.
FCL (Forceps, Biopsy, Non-Electric), HFB (Forceps, Biopsy, Gynecological), PTS (Endoscopic grasping/cutting instrument, non-powered, exempt), FCL (FORCEPS, BIOPSY, NON-ELECTRIC)
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.