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Vibrance Pelvic Trainer

by Bioinfinity (M) Sdn. Bhd.

510(k) K162689

Vibrance Pelvic Trainer is a Class II device made by Bioinfinity (M) Sdn. Bhd., cleared under FDA 510(k) K162689 on 8 Jun 2017, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK162689 Date8 Jun 2017ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
HIR
Device class
Class II
Regulation
21 CFR Part 884.1425
Advisory committee
Obstetrics/Gynecology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code HIR (Perineometer).

Other devices from Bioinfinity (M) Sdn. Bhd.