Collagen Shield for Acute Care

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K913148 ↗

FDA Product Code

MOE

Device Class

Class I

Regulation

21 CFR Part 886.4750

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Vitachoice Wound Dressing

  Class I

  FDA 510(k) K896455 Active Cleared 15 Feb 1990

• Vitaaccess (Tm) Catheter Introducer System

  Class II

  FDA 510(k) K872998 Active Cleared 24 Mar 1988

• Vitaaccess Catheter Introducer Kit

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  FDA 510(k) K890435 Active Cleared 29 Mar 1989

• Vitapatch Cath. Securement Device W/Chlorhexidine

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  FDA 510(k) K896046 Active Cleared 11 Jan 1990

• Vitapatch Pin Protection Device for Percut. Pins

  Class II

  FDA 510(k) K872538 Active Cleared 10 Jul 1987

• Collagen Neurosponge

  Class II

  FDA 510(k) K891993 Active Cleared 23 Mar 1990

See all devices from Vitaphore Corp. →