# Optik

- Location (FDA's records): Criftib, MD
- FDA decisions: 6 (1989–1994): 6 510(k) clearances
- Product codes: JEY (1), HRW (1), FWF (1), GCJ (1), LRZ (1), HRX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Solos Endoscopy, Inc.: 1 (https://510kreport.com/company/solos-endoscopy)

## Its most-cited devices
- K926166: Coast Video Endoscopic Imaging System (1993), cited by 1

## Recent decisions
- K933776: Optik Laparoscope (Mar 16, 1994)
- K926166: Coast Video Endoscopic Imaging System (Jun 1, 1993)
- K896404: Titamed Antwerp System (Apr 16, 1990)
- K896589: Manual Surgical Instruments for Titamed Antwerp (Dec 27, 1989)
- K894557: Lightscope Set (Aug 7, 1989)
- K894558: Mini Lightscope Set, Lightscope JR. Set (Aug 7, 1989)

Source page: https://510kreport.com/company/optik