# Innervision, Inc.

- Location (FDA's records): Memphis, TN
- FDA decisions: 6 (1994–1999): 6 510(k) clearances
- Product codes: HET (2), GEI (2), GCJ (1), JDS (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
- K992345: Christoudias Slim Tip Electrode Insert (Sep 10, 1999)
- K991877: Macmed Paediatric Intramedullary Nail (Aug 6, 1999)
- K982428: Christoudias Gauze Dissector (Laparoscopic Hand Instrument) (Oct 9, 1998)
- K940731: Innervision Inc. Cannula/Trocar,Multiple Types (Sep 13, 1994)
- K940750: Innervision,Inc. Laparoscopic Electrodes (Aug 23, 1994)
- K940718: Innervision Inc. Laparoscopic Hand Instruments (Jul 22, 1994)

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