A non-bioabsorbable clip intended to be implanted long-term (>30 days) within the gastrointestinal (GI) tract during an endoscopic procedure for endoscopic marking, haemostasis, tissue approximation, closure of luminal perforations, treating mucosal/submucosal
| Company | Devices | Share |
|---|---|---|
| Micro-Tech (Nanjing) Co., Ltd. | 97 | 49% |
| Ovesco Endoscopy Ag | 23 | 12% |
| Ovesco Endoscopy Usa, Inc. | 20 | 10% |
| Anrei Medical(Hz) Co.,Ltd. | 13 | 7% |
| Yangzhou Fartley Medical Instrument Technology Co., Ltd | 12 | 6% |
| Us Endoscopy | 11 | 6% |
| Alton (Shanghai) Medical Instruments Co., Ltd. | 8 | 4% |
| Boston Scientific Corporation | 6 | 3% |
| Jiangsu Vedkang Medical Science And Technology Co.,Ltd. | 3 | 2% |
| Medeon Biodesign, Inc. | 2 | 1% |
| Cook Incorporated | 2 | 1% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| PKL | Hemostatic Metal Clip For The Gi Tract | 189 |
| PKL | Hemostatic metal clip for the GI tract | 23 |
| PLK | Tympanic Membrane Direct Contact Hearing Aid | 6 |
| OCZ | Endoscopic Grasping/Cutting Instrument, Non-Powered | 3 |
| HCF | Instrument, Ligature Passing And Knot Tying | 2 |
| GCJ | Laparoscope, General & Plastic Surgery | 2 |
Use these as the dimensions to specify in a tender line.
197 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Gastrointestinal endoscopic clip, long-term, non-bioabsorbable", from 11 companies. The largest labeler is Micro-Tech (Nanjing) Co., Ltd. with 49% of records.
PKL (Hemostatic Metal Clip For The Gi Tract), PKL (Hemostatic metal clip for the GI tract), PLK (Tympanic Membrane Direct Contact Hearing Aid), OCZ (Endoscopic Grasping/Cutting Instrument, Non-Powered)
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.