510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K083721Substantially Equivalent

Modification to Zenieva

River'S Edge Pharmaceuticals, LLC, Durham NC / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083721 is the FDA 510(k) clearance record for MODIFICATION TO ZENIEVA, a class I device, cleared for River'S Edge Pharmaceuticals, LLC on under FDA product code NAE (Dressing, Wound, Hydrogel Without Drug And/Or Biologic). FDA records list one 510(k) clearance for River'S Edge Pharmaceuticals, LLC. As of , FDA records show no recalls naming K083721.

Clearance record

Decision date
Received
(24 days to decision)
Product code
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic
Regulation
21 CFR 878.4022
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
River'S Edge Pharmaceuticals, LLC 2445 S. Alston Ave., Durham NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NAE

Trailing 12 months

FDA records hold no clearances under product code NAE in the trailing twelve months.

FDA records show no clearances under product code NAE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NAE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260