# Lori Medical Laboratories, Inc.

- Location (FDA's records): Golden Valley, MN
- FDA decisions: 8 (1989–1997): 8 510(k) clearances
- Product codes: ESD (7), KHL (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
- K973376: Lori/Lori, Lori-S (Lori Stock Aid) (Oct 14, 1997)
- K972058: Loripro, Loripro II (Aug 15, 1997)
- K964080: Lori Hearing Aid Simulator (Jan 8, 1997)
- K952711: LORI-A (Jul 3, 1995)
- K940639: Lori-Cic Hearing Aid (Mar 25, 1994)
- K893723: Lori-Model L, Canal in-the-Ear Instrument (Sep 8, 1989)
- K893722: Lori-Model H, Half Concha in-the-Ear Instrument (Sep 8, 1989)
- K893721: Lori-Model O, Low Profile in-the Ear Instrument (Sep 8, 1989)

Source page: https://510kreport.com/company/lori-medical-laboratories