510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K201523Substantially Equivalent

Sharps container

Zhejiang Gongdong Medical Technology Co., Ltd, Taizhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K201523 is the FDA 510(k) clearance record for Sharps container, a class II device, cleared for Zhejiang Gongdong Medical Technology Co., Ltd. on under FDA product code MMK (Container, Sharps). FDA records list 3 510(k) clearances for Zhejiang Gongdong Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K201523.

Clearance record

Decision date
Received
(157 days to decision)
Product code
MMK Container, Sharps
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Zhejiang Gongdong Medical Technology Co., Ltd. #10 Beiyuan Ave., Huangyan, Taizhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MMK

Trailing 12 months
3 clearances under product code MMK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MMK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20261
September 20260
October 20260