510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K834367Substantially Equivalent

Suture Removal Wound Closure-Instru-

Sterling Multi-Products, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834367 is the FDA 510(k) clearance record for SUTURE REMOVAL WOUND CLOSURE-INSTRU-, a class I device, cleared for Sterling Multi-Products, Inc. on under FDA product code HTD (Forceps). FDA records list one 510(k) clearance for Sterling Multi-Products, Inc. As of , FDA records show no recalls naming K834367.

Clearance record

Decision date
Received
(173 days to decision)
Product code
HTD Forceps
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Sterling Multi-Products, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HTD

Trailing 12 months

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

FDA records show no clearances under product code HTD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HTD, 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