510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K982626Substantially Equivalent

Urethropexy Suture Placement Kit Model Numbers Um-300, Mw-100, Mini-Laparotomy Mmk Kit Model Um-250, Laparoscopic Burch0

Medworks Corp., Pawtucket RI / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K982626 is the FDA 510(k) clearance record for URETHROPEXY SUTURE PLACEMENT KIT MODEL NUMBERS UM-300, MW-100, MINI-LAPAROTOMY MMK KIT MODEL UM-250, LAPAROSCOPIC BURCH0, a class II device, cleared for Medworks Corp. on under FDA product code EZL (Catheter, Retention Type, Balloon). FDA records list 3 510(k) clearances for Medworks Corp., from to . As of , FDA records show no recalls naming K982626.

Clearance record

Decision date
Received
(23 days to decision)
Product code
EZL Catheter, Retention Type, Balloon
Regulation
21 CFR 876.5130
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medworks Corp. 50 Brewster St., Pawtucket RI
510(k) summary
Summary
Third party review
No

Clearances, product code EZL

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