# LimFlow, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 7 (2022–2026): 6 510(k) clearances and 1 original PMA approval
- Product codes: MGZ (2), MMX (2), PDU (2), QWN (1)
- 510(k) review time since 2016: median 29 days, against 139 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- LeMaitre Vascular, Inc.: 1 (https://510kreport.com/company/lemaitre-vascular)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Cordis Corp., A Johnson & Johnson Co.: 1 (https://510kreport.com/company/cordis-a-johnson-johnson)

## Its most-cited devices
- K221902: LimFlow Vector (2022), cited by 1
- K222083: LimFlow V-Ceiver (2022), cited by 1
- K221541: LimFlow ARC (2022), cited by 1

## Recent decisions
- K260188: LimFlow Vector (Mar 18, 2026)
- K251376: LimFlow ARC (May 31, 2025)
- K242776: LimFlow V-Ceiver (Feb 14, 2025)
- P220025: LimFlow System (Sep 11, 2023)
- K221902: LimFlow Vector (Dec 21, 2022)
- K221541: LimFlow ARC (Aug 31, 2022)
- K222083: LimFlow V-Ceiver (Aug 9, 2022)

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