# ZEISS

- Location (FDA's records): Mchenry, IL
- FDA decisions: 2 (1982–1982): 2 510(k) clearances
- Product codes: HQG (1), GEI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K822573: Sunglass Lenses (Oct 22, 1982)
- K821263: Select Bipolar Coagulation Forceps (Jun 10, 1982)

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