510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935235Substantially Equivalent

Endoscopy System for Facial Plastic Surgery

Smith & Nephew Richards, Inc., Bartlett TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935235 is the FDA 510(k) clearance record for ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY, a class II device, cleared for Smith & Nephew Richards, Inc. on under FDA product code GCM (Endoscope, Rigid). FDA records list 87 510(k) clearances for Smith & Nephew Richards, Inc., from to . As of , FDA records show no recalls naming K935235.

Clearance record

Decision date
Received
(507 days to decision)
Product code
GCM Endoscope, Rigid
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Smith & Nephew Richards, Inc. 2925 Appling Rd., Bartlett TN
510(k) summary
Summary
Third party review
No

Clearances, product code GCM

Trailing 12 months

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

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