510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864384Substantially Equivalent

Luxtec Retractors, Luxtec Specialty Retractors

Luxtec Corp., Sturbridge MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864384 is the FDA 510(k) clearance record for LUXTEC RETRACTORS, LUXTEC SPECIALTY RETRACTORS, a class I device, cleared for Luxtec Corp. on under FDA product code GAD (Retractor). FDA records list 15 510(k) clearances for Luxtec Corp., from to . As of , FDA records show no recalls naming K864384.

Clearance record

Decision date
Received
(14 days to decision)
Product code
GAD Retractor
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Luxtec Corp. P.O. Box 225, Rte. 20/49, Sturbridge MA
Third party review
No

Clearances, product code GAD

Trailing 12 months

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

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