510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K000728Substantially Equivalent

Medtronic Solan Fiberoptic Corneal Light Probe

Medtronic Xomed, Inc., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000728 is the FDA 510(k) clearance record for MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE, a class II device, cleared for Medtronic Xomed on under FDA product code FST (Light, Surgical, Fiberoptic). FDA records list 46 510(k) clearances for Medtronic Xomed, from to . As of , FDA records show no recalls naming K000728.

Clearance record

Decision date
Received
(15 days to decision)
Product code
FST Light, Surgical, Fiberoptic
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medtronic Xomed 6743 Southpoint Dr. N., Jacksonville FL
510(k) summary
Summary
Third party review
Yes

Clearances, product code FST

Trailing 12 months

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

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