# Candulor USA, Inc.

- Location (FDA's records): Amherst, NY
- FDA decisions: 2 (2010–2012): 2 510(k) clearances
- Product codes: ELM (1), EBG (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
- K122852: Physiostar NFC (Dec 6, 2012)
- K101814: Direct Crown Natural 1 (Sep 27, 2010)

Source page: https://510kreport.com/company/candulor-usa