# Fci Ophthalmics, Inc.

- Location (FDA's records): Marshfield Hills, MA
- FDA decisions: 13 (1996–2006): 13 510(k) clearances
- Product codes: OKS (4), LZU (3), HQX (2), HPZ (2), MQU (1), HJK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Fci (France Chirurgie Instrumentation) Sas: 4 (https://510kreport.com/company/fci-france-chirurgie-instrumentation)
- Hiroyasu Higuchi: 2 (https://510kreport.com/company/hiroyasu-higuchi)
- Dcs Surgical, Inc.: 1 (https://510kreport.com/company/dcs-surgical)

## Its most-cited devices
- K061404: Mono-Crawford Naso-Lacrimal Intubation Device (2006), cited by 3
- K991238: Fci Crawford Probe Intubation Sets (1999), cited by 2
- K041869: Self Retaining Bicanaliculus Intubation Set (2004), cited by 2

## Recent decisions
- K061404: Mono-Crawford Naso-Lacrimal Intubation Device (Aug 7, 2006)
- K061398: Snug Plug Punctum Plug (Jul 11, 2006)
- K041869: Self Retaining Bicanaliculus Intubation Set (Nov 18, 2004)
- K023758: Becker Transnasal Lacrimal (Intubation Sets) (Sep 17, 2003)
- K023400: Fci Mesh Wrapped Bioceramic Orbital Implant (Aug 22, 2003)
- K030054: Disposable Vitrectomy Sets, Disposable Virectomy Lenses (Feb 26, 2003)
- K992294: Bioceramic Orbital Implant (Apr 19, 2000)
- K991238: Fci Crawford Probe Intubation Sets (Jul 8, 1999)

Source page: https://510kreport.com/company/fci-ophthalmics