Orthopedic Forceps

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K780397 ↗

FDA Product Code

HTX

Device Class

Class I

Regulation

21 CFR Part 888.4540

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

• Wheelchair Muff

  Class I

  FDA 510(k) K780195 Active Cleared 9 Mar 1978

• Strap, Legrest

  Class I

  FDA 510(k) K780191 Active Cleared 14 Feb 1978

• Threaded Rod Clamp

  Class I

  FDA 510(k) K781447 Active Cleared 27 Sep 1978

• Wheelchair Accessories

  Class I

  FDA 510(k) K780184 Active Cleared 13 Feb 1978

• Cup, Acetabular, Long Posterior Wall

  Class II

  FDA 510(k) K780398 Active Cleared 21 Mar 1978

• Flat Wrench

  Class I

  FDA 510(k) K781451 Active Cleared 27 Sep 1978

See all devices from Orthopedic Equipment Co., Inc. →