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Coreva Health Science, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3006324197

Devices
0
Registrations
FDA
FDA recalls
1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3006324197
Address
2985 E Hillcrest Dr Ste 205, Westlake Village, CA, 91362

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2015

    • 18 May 2015 Z-1697-2015 Class II Terminated Coreva Health Science, LLC. is recalling ActCel Hemostatic Dressing due to customer literature and web sites promoting that it can help control bleeding from open wounds and in body cavities. ActCel is indicated as a prescription device for management of topical wounds and to temporarily control external surface bleeding. Distribution: U.S. distribution to the following; TX, NY, FL, VA, WA, and AZ. No foreign distribution. NOTE: The distribution list the…
      Full distribution text U.S. distribution to the following; TX, NY, FL, VA, WA, and AZ. No foreign distribution. NOTE: The distribution list the firm provided does not include all consignees that purchased the product; rather target the consignees (distributors) who were observed to be using an unapproved marketing use.
      Submission number: K112800

This is an FDA establishment record without devices in deviCERTS.