# Loredan Biomedical, Inc.

- Location (FDA's records): Davis, CA
- FDA decisions: 9 (1983–1993): 9 510(k) clearances
- Product codes: IKK (7), BXB (1), LXJ (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
- K924512: Lido V-Tak (May 12, 1993)
- K924513: Lido (R) Linea (Mar 31, 1993)
- K903429: Lido Linea (Aug 14, 1990)
- K884487: Lido TM Active Back (Nov 18, 1988)
- K880017: Lido (TM) Lift (Feb 26, 1988)
- K880018: Lido (TM) Workset (Feb 26, 1988)
- K871793: Lido Active (Jun 5, 1987)
- K861986: Lido Back (Jun 2, 1986)

Source page: https://510kreport.com/company/loredan-biomedical