510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012685Substantially Equivalent

Reprocessed Endoscopic Electrodes

Sterilmed Inc, Maple Grove MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012685 is the FDA 510(k) clearance record for REPROCESSED ENDOSCOPIC ELECTRODES, a class II device, cleared for Sterilmed, Inc. on under FDA product code NLW (Electrode, Electrosurgical, Active, Urological, Reprocessed). FDA's definition for product code NLW reads: "The "electrode, electrosurgical, active, urological, reprocessed" is intended to be used endoscopically to contact urologic tissue so as to allow cutting, coagulation, electrodesiccation, or cautery dessication by means of electric...". FDA records list 65 510(k) clearances for Sterilmed, Inc., from to . As of , FDA records show one recall naming K012685.

Clearance record

Decision date
Received
(184 days to decision)
Product code
NLW Electrode, Electrosurgical, Active, Urological, Reprocessed
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Sterilmed, Inc. 11400 73rd Ave. N, Maple Grove MN
510(k) summary
Summary
Third party review
No

Clearances, product code NLW

Trailing 12 months

FDA records hold no clearances under product code NLW in the trailing twelve months.

FDA records show no clearances under product code NLW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NLW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260