# Medicore, Inc.

- Location (FDA's records): Hialeah, FL
- FDA decisions: 6 (1981–2021): 6 510(k) clearances
- Names in FDA's records: Medicore, Inc. (3); Medicore Co., Ltd. (3)
- Product codes: FMK (2), JOM (2), LHQ (1), FMF (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Meridian AG: 2 (https://510kreport.com/company/meridian)
- Meditherm, Inc.: 1 (https://510kreport.com/company/meditherm)

## Firms that cite its devices most
- Medtechs, LLC: 1 (https://510kreport.com/company/medtechs)

## Its most-cited devices
- K073323: SA-3000P (2007), cited by 1

## Recent decisions
- K212412: Iris-XP (Sep 13, 2021)
- K110374: Max Pulse System (Jun 13, 2011)
- K073323: SA-3000P (Nov 29, 2007)
- K983430: Lite-Touch Syringe (Feb 9, 1999)
- K880869: Medi-Let (Mar 21, 1988)
- K810681: Medi-Lance (Mar 26, 1981)

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