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Femidom Single-Use Internal Condom

by The Female Health Co.

PMA P940033

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 14 Apr 1995

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP940033 Date14 Apr 1995Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Full name
Femidom
Generic Name
Single-use internal condom
PMA Number
FDA Product Code
MBU
Device Class
Class II
Regulation
21 CFR Part 884.5340
Advisory Committee
Obstetrics/Gynecology
FDA Decision
APWD Approval withdrawn

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