# Damor America, Inc.

- Location (FDA's records): Washington, D.C., DC
- FDA decisions: 4 (1989–1993): 4 510(k) clearances
- Product codes: MGQ (2), FRO (1), IRP (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
- K933328: Damor Creme (Dec 7, 1993)
- K934267: Damor Cream Saturated Dressing (Dec 7, 1993)
- K901022: Powered Inflatable Tube Massager, Sport-Med (Mar 14, 1990)
- K891097: Damor Cream Saturated Dressing (Aug 25, 1989)

Source page: https://510kreport.com/company/damor-america