Devon Knee Strap

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K760950 ↗

FDA Product Code

IQI

Device Class

Class I

Regulation

21 CFR Part 890.3475

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Magnetic Drape - Instrument Holder

  Class II

  FDA 510(k) K780865 Active Cleared 21 Aug 1978

• Sponge Counter

  Class I

  FDA 510(k) K790538 Active Cleared 4 Apr 1979

• Electrosurgical Tip Cleaner & Holder

  Class II

  FDA 510(k) K803055 Active Cleared 12 Feb 1981

• Surgical Instrument Protector

  Class II

  FDA 510(k) K771123 Active Cleared 28 Oct 1977

• The Sharps Collection and Disposal System

  Class II

  FDA 510(k) K945197 Active Cleared 2 Dec 1994

• Easy-On

  Class I

  FDA 510(k) K932998 Active Cleared 18 Aug 1993

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