A sterile, hand-held, manual, ophthalmic surgical instrument intended to be used to cut intraocular tissue (e.g., during anterior chamber surgery, vitrectomy). As a complete instrument it comprises two shearing blades at the end of a probe-/cannula-like shaft
| Company | Devices | Share |
|---|---|---|
| Katalyst Surgical Llc | 17 | 33% |
| Alcon Laboratories, Inc. | 13 | 25% |
| Vitreq B.V. | 8 | 16% |
| D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. | 8 | 16% |
| Geuder Aktiengesellschaft | 2 | 4% |
| Fci S A S Fci 20 22 | 2 | 4% |
| Dtr Medical Limited | 1 | 2% |
Company = labeler of record on GUDID. 7 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 |
|---|---|---|
| HNF | Scissors, Ophthalmic | 48 |
| HNF | SCISSORS, OPHTHALMIC | 13 |
| HNR | Forceps, Ophthalmic | 2 |
Use these as the dimensions to specify in a tender line.
51 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intraocular scissors, probe-like, single-use", from 7 companies. The largest labeler is Katalyst Surgical Llc with 33% of records.
HNF (Scissors, Ophthalmic), HNF (SCISSORS, OPHTHALMIC), HNR (Forceps, Ophthalmic)
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.