# Denar Corp.

- Location (FDA's records): Anaheim, CA
- FDA decisions: 5 (1985–1992): 5 510(k) clearances
- Product codes: DZE (3), IZT (1), IWY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (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 that cite its devices most
- Drm Research Laboratories, Inc.: 2 (https://510kreport.com/company/drm-research-laboratories)
- Crystal Medical Technology: 2 (https://510kreport.com/company/crystal-medical-technology)
- Quantum Bioengineering, Ltd.: 2 (https://510kreport.com/company/quantum-bioengineering)
- Dentatus USA, Ltd.: 2 (https://510kreport.com/company/dentatus-usa)

## Its most-cited devices
- K852802: Denar Dental Implant (1985), cited by 4
- K884845: Steri-Oss (1989), cited by 4

## Recent decisions
- K925705: Accurad-200 System & Accurad-300 Plus System (Dec 28, 1992)
- K924759: Collimator Light Source (Dec 9, 1992)
- K884845: Steri-Oss (Feb 10, 1989)
- K883373: Steri-Oss Hydroxyapatite-Coated Dental Implant (Jan 13, 1989)
- K852802: Denar Dental Implant (Sep 23, 1985)

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