# Oculo Plastik, Inc.

- Location (FDA's records): Montreal, Quebec Canada, CA
- FDA decisions: 13 (1990–2013): 13 510(k) clearances
- Names in FDA's records: Oculo Plastik, Inc. (12); Oculo-Plastik, Inc. (1)
- Product codes: HPZ (8), HQX (5)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 5 (2 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
- Evera Medical, Inc.: 1 (https://510kreport.com/company/evera-medical)
- Becker & Associates Consulting, Inc.: 1 (https://510kreport.com/company/becker-associates-consulting)
- Bio-Vascular, Inc.: 1 (https://510kreport.com/company/bio-vascular)

## Its most-cited devices
- K934834: Eptfe Sheet Covering for Ocular Implant (1994), cited by 3
- K073293: Durette Implant (2008), cited by 1
- K040689: Eye Sphere Implants (2004), cited by 1

## Recent decisions
- K123764: Durette Ocular Implant (Jan 31, 2013)
- K112176: Silicone Spheres (Sep 15, 2011)
- K073293: Durette Implant (Mar 19, 2008)
- K040689: Eye Sphere Implants (Jun 10, 2004)
- K934834: Eptfe Sheet Covering for Ocular Implant (May 5, 1994)
- K915630: Ophtimplant (Mar 2, 1992)
- K901002: O'donnell, Socket Reconstruction Prostheses (May 22, 1990)
- K900929: Putterman-Scott, Socket Reconstruction Bilateral (May 18, 1990)

Source page: https://510kreport.com/company/oculo-plastik