# Coburn Optical Ind., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1978–1989): 14 510(k) clearances
- Product codes: HJG (5), HQE (2), HPJ (1), GES (1), HQF (1), HQG (1), HPT (1), HKP (1), HJO (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
- K892349: Magnilink System 209 (May 26, 1989)
- K892350: Magnilink System 402/5 (May 26, 1989)
- K892351: Magnilink System 602 (May 26, 1989)
- K892348: Magnilink System 201 (May 26, 1989)
- K892347: Magnilink System 101 (May 26, 1989)
- K862188: Irrigation & Aspiration/Vitrectomy Device (Aug 21, 1986)
- K853457: Coburn I/a System (Oct 15, 1985)
- K821737: Disp. Microsurgical Knives (Jul 2, 1982)

Source page: https://510kreport.com/company/coburn-optical-ind