# Almore Intl., Inc.

- Location (FDA's records): Portland, OR
- FDA decisions: 21 (1980–1986): 21 510(k) clearances
- Product codes: EJL (2), HTD (2), EJP (2), HKC (1), EEG (1), JEP (1), KCR (1), ECB (1), EKQ (1), JES (1), EAX (1), HJH (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
- K862851: Almore Face Mask (Aug 12, 1986)
- K854692: Monarch II Bleaching Instrument (May 12, 1986)
- K854696: OP II Visible Light Curing System (Mar 26, 1986)
- K854690: Diamonds Burs-Composit Finishing (Mar 25, 1986)
- K854691: Diamond Burs-Handpiece (Mar 25, 1986)
- K854700: EZ-on Tubing Conditioner (Lubricant) (Mar 12, 1986)
- K854701: Retract-a-Cord (Mar 6, 1986)
- K854697: Tubing Handpiece Replacement (Mar 6, 1986)

Source page: https://510kreport.com/company/almore-intl