510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993314Substantially Equivalent

Synthes Light Guide

Synthes (USA) Products LLC, West Chester PA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K993314 is the FDA 510(k) clearance record for SYNTHES LIGHT GUIDE, a class II device, cleared for Synthes (Usa) on under FDA product code FQP (Lamp, Operating-Room). FDA records list 479 510(k) clearances for Synthes (USA) Products LLC, from to . As of , FDA records show no recalls naming K993314.

Clearance record

Decision date
Received
(63 days to decision)
Product code
FQP Lamp, Operating-Room
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Synthes (Usa) 1303 Goshen Pkwy., West Chester PA
510(k) summary
Summary
Third party review
No

Clearances, product code FQP

Trailing 12 months

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

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