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Flexmate K500

by Breg, Inc.

510(k) K950755

Flexmate K500 is a medical device (FDA Class I; FDA product code BXB, Exerciser, Powered) made by Breg, Inc., cleared under FDA 510(k) K950755 on 5 Oct 1995, 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 NumberK950755 Date5 Oct 1995ClearedStatusActive

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  • Withdrawn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
BXB
Device class
Class I
Regulation
21 CFR Part 890.5380
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code BXB (Exerciser, Powered).

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