ClearanceBrief
Company ยท KR

Weero Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (2 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IPFStimulator, Muscle, Powered3
PBXMassager, Vacuum, Radio Frequency Induced Heat3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 8, 2026K253542Apollo Quattro (APQ-10M)
Weero Co., Ltd., KR
IPF
Mar 13, 2026K253261Apollo Quattro (APQ-10M)
Weero Co., Ltd., KR
PBX
Jun 4, 2025K241433EVE Synergy (EVE-20M)
Weero Co., Ltd., KR
IPF
Oct 10, 2024K240992eMVFit (MVF-10M)
Weero Co., Ltd., KR
IPF
Oct 9, 2024K240991eMVFit (MVF-10M)
Weero Co., Ltd., KR
PBX
Aug 25, 2022K212253Apollo Duet (Model : APD-4000)
Weero Co., KR
PBX

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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