# Velmeni, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 4 (2024–2026): 4 510(k) clearances
- Product codes: MYN (3), QIH (1)
- 510(k) review time since 2016: median 216 days, against 130 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Overjet, Inc.: 1 (https://510kreport.com/company/overjet)
- Pearl, Inc.: 1 (https://510kreport.com/company/pearl)

## Its most-cited devices
- K240003: Velmeni for Dentists (V4D) (2024), cited by 2

## Recent decisions
- K254096: VELMENI for DENTISTS (V4D) 3D (Jul 23, 2026)
- K252953: Velmeni for Dentists (V4D)  Endo-Perio (May 11, 2026)
- K250753: VELMENI for DENTISTS (V4D) (Sep 2, 2025)
- K240003: Velmeni for Dentists (V4D) (Aug 30, 2024)

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