# Surgidev Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1983–1985): 4 510(k) clearances
- Product codes: HLR (1), FRN (1), HNN (1), HIX (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
- K850729: Acuflo Volumetric Controlled Delivery Sys 2000 (Apr 9, 1985)
- K831829: Karickhoff Flying Corpuscle Viewer (Oct 19, 1983)
- K831975: Leading Edge Ophthalmic Knife (Aug 31, 1983)
- K830008: Karickhoff Keratoscope (Jan 26, 1983)

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