# Revvity, Inc.

- Location (FDA's records): Waltham
- FDA decisions: 2 (1998–2026): 1 510(k) clearance and 1 original PMA approval
- Product codes: LOK (1), QUE (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Perkinelmer, Inc.: 1 (https://510kreport.com/company/perkinelmer)

## Recent decisions
- K262893: Eonis™ SMA kit (Sep 30, 2026)
- P970037: Autodelfia Hafp Test Kit (Mar 31, 1998)

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