# Weero Co., Ltd.

- Location (FDA's records): Suwon, KR
- FDA decisions: 6 (2022–2026): 6 510(k) clearances
- Names in FDA's records: Weero Co., Ltd. (5); Weero Co. (1)
- Product codes: IPF (3), PBX (3)
- 510(k) review time since 2016: median 194 days, against 216 for FDA's reviews in the same codes and years (2 of 6 faster)
- Predicates its devices cite: 11 (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
- InMode, Ltd.: 5 (https://510kreport.com/company/inmode)
- Inmode MD, Ltd.: 2 (https://510kreport.com/company/inmode-md)
- Timewaver Production GmbH: 1 (https://510kreport.com/company/timewaver-production)
- R2 Technologies, Inc.: 1 (https://510kreport.com/company/r2-technologies)

## Its most-cited devices
- K241433: EVE Synergy (EVE-20M) (2025), cited by 1
- K212253: Apollo Duet (Model : APD-4000) (2022), cited by 1

## Recent decisions
- K253542: Apollo Quattro (APQ-10M) (Jun 8, 2026)
- K253261: Apollo Quattro (APQ-10M) (Mar 13, 2026)
- K241433: EVE Synergy (EVE-20M) (Jun 4, 2025)
- K240992: eMVFit (MVF-10M) (Oct 10, 2024)
- K240991: eMVFit (MVF-10M) (Oct 9, 2024)
- K212253: Apollo Duet (Model : APD-4000) (Aug 25, 2022)

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