510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K053538Substantially Equivalent

Modification to Phytacare Alginate Hydrogel Wound Filler

Curapharm, Inc., Santee CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K053538 is the FDA 510(k) clearance record for MODIFICATION TO PHYTACARE ALGINATE HYDROGEL WOUND FILLER, cleared for Curapharm, Inc. on under FDA product code FRO (Dressing, Wound, Drug). FDA records list one 510(k) clearance for Curapharm, Inc. As of , FDA records show no recalls naming K053538.

Clearance record

Decision date
Received
(294 days to decision)
Product code
FRO Dressing, Wound, Drug
Device class
Unclassified
Review panel
Unknown
Applicant
Curapharm, Inc. 10054 Prospect Ave., Suite F, Santee CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FRO

Trailing 12 months
19 clearances under product code FRO in the twelve months to October 2026, January 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FRO, trailing twelve months
MonthClearances
November 20251
December 20251
January 20264
February 20261
March 20263
April 20261
May 20261
June 20263
July 20260
August 20262
September 20262
October 20260