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EnPlace

FEMSELECT LTD · Model FG-00001-02 · UDI-DI 07290017082028

PBQ Prescription
1
510(k) clearances
66
Adverse events
1
Recalls
9
Facilities

Recalls

DateFirmReason
2021-12-13FEMSelect LtdCertain lots may not have been packaged wth the Channel Tube Limiter.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.