# Endooptiks, Inc.

- Location (FDA's records): Little Silver, NJ
- FDA decisions: 5 (1992–2009): 5 510(k) clearances
- Product codes: GEX (3), EYB (1), EOB (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Firms that cite its devices most
- Beaver Visitec International, Inc.: 1 (https://510kreport.com/company/beaver-visitec-international)

## Its most-cited devices
- K042918: Microprobe Laser and Endoscopy System, Model E2 (2004), cited by 1

## Recent decisions
- K083788: Endo Optiks Urological Catheter for Endoscopy, Model Sessr (Mar 3, 2009)
- K042918: Microprobe Laser and Endoscopy System, Model E2 (Nov 22, 2004)
- K003151: Micropobe Series of Lasers and Accessories (Jan 8, 2001)
- K945081: Transtympanic Endoscope (Mar 6, 1995)
- K922917: Endoprobes (Sep 28, 1992)

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