A flexible device intended to access the gastrointestinal (GI) tract, and/or the airway tree, via the working channel of an appropriate endoscope to atraumatically remove foreign bodies during an endoscopic procedure; it may in addition be intended for removal
| Company | Devices | Share |
|---|---|---|
| Beijing Zksk Technology Co.,Ltd | 72 | 52% |
| Us Endoscopy | 23 | 17% |
| Endo-Therapeutics, Inc. | 16 | 12% |
| Olympus Medical Systems Corp. | 6 | 4% |
| Karl Storz Gmbh & Co. Kg | 4 | 3% |
| Diversatek Healthcare, Inc. | 4 | 3% |
| Conmed Corporation | 4 | 3% |
| Boston Scientific Corporation | 4 | 3% |
| Telemed Systems | 3 | 2% |
| Cook Incorporated | 2 | 1% |
| Gt Metabolic Solutions, Inc. | 1 | 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 |
|---|---|---|
| PTS | Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt | 74 |
| GCJ | Laparoscope, general & plastic surgery | 47 |
| FDI | SNARE, FLEXIBLE | 46 |
| OCZ | Endoscopic Grasping/Cutting Instrument, Non-Powered | 27 |
| FGX | Snare, Non-Electrical | 18 |
| KTI | Bronchoscope Accessory | 4 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
139 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Gastrointestinal/airway foreign body retrieval basket, single-use", from 11 companies. The largest labeler is Beijing Zksk Technology Co.,Ltd with 52% of records.
PTS (Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt), GCJ (Laparoscope, general & plastic surgery), FDI (SNARE, FLEXIBLE), 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.