510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252021Substantially Equivalent

Disposable Endoscopic Injection Needles

Changzhou New Med Micro-Medtech Co., Ltd., Changzhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252021 is the FDA 510(k) clearance record for Disposable Endoscopic Injection Needles, a class II device, cleared for Changzhou New Med Micro-Medtech Co., Ltd. on under FDA product code FBK (Endoscopic Injection Needle, Gastroenterology-Urology). FDA's definition for product code FBK reads: "inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue". FDA records list one 510(k) clearance for Changzhou New Med Micro-Medtech Co., Ltd. As of , FDA records show no recalls naming K252021.

Clearance record

Decision date
Received
(155 days to decision)
Product code
FBK Endoscopic Injection Needle, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Changzhou New Med Micro-Medtech Co., Ltd. # 99 Of Longxi Ave., Zhulin Town, Jintan District,, Changzhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FBK

Trailing 12 months
3 clearances under product code FBK 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 FBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260