# Km Corporation

- Location (FDA's records): Anaheim, CA
- FDA decisions: 4 (2014–2024): 4 510(k) clearances
- Names in FDA's records: Km Corporation (3); Km Corp. (1)
- Product codes: KIF (2), FRG (1), EBF (1)
- Predicates its devices cite: 8 (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

## Firms whose devices it cites most
- Meta Biomed Co., Ltd.: 3 (https://510kreport.com/company/meta-biomed)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)
- Sigma Medical Supplies Corp.: 1 (https://510kreport.com/company/sigma-medical-supplies)
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)
- GC America, Inc.: 1 (https://510kreport.com/company/gc-america)
- Vericom Co., Ltd.: 1 (https://510kreport.com/company/vericom)

## Recent decisions
- K241123: Perpak™ Sterilization Tyvek Pouch (Sep 18, 2024)
- K140976: Enaden Flow (Jul 10, 2014)
- K133716: TRC-Paste (Apr 9, 2014)
- K132123: TRC-Pex, Radic-Sealer (Mar 20, 2014)

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