510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211809Substantially Equivalent

Surgical Gown

Wuhan Dymex Healthcare Co., Ltd., Wuhan, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211809 is the FDA 510(k) clearance record for Surgical Gown, a class II device, cleared for Wuhan Dymex Healthcare Co., Ltd. on under FDA product code FYA (Gown, Surgical). FDA records list 4 510(k) clearances for Wuhan Dymex Healthcare Co., Ltd., from to . As of , FDA records show no recalls naming K211809.

Clearance record

Decision date
Received
(129 days to decision)
Product code
FYA Gown, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Wuhan Dymex Healthcare Co., Ltd. Rm. 1701, Unit 2, Bldg. 5, Jinsegangwan Phase 5,, Wuhan, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FYA

Trailing 12 months
10 clearances under product code FYA in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FYA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20262
March 20260
April 20262
May 20261
June 20261
July 20261
August 20262
September 20260
October 20260