510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K810409Substantially Equivalent

Model C2100-Series Ophthalmic Cryoprobe

Medtronic, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810409 is the FDA 510(k) clearance record for MODEL C2100-SERIES OPHTHALMIC CRYOPROBE, a class II device, cleared for Valleylab, Inc. on under FDA product code GEH (Unit, Cryosurgical, Accessories). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K810409.

Clearance record

Decision date
Received
(30 days to decision)
Product code
GEH Unit, Cryosurgical, Accessories
Regulation
21 CFR 878.4350
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Valleylab, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GEH

Trailing 12 months
9 clearances under product code GEH in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GEH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20262
March 20260
April 20262
May 20260
June 20262
July 20260
August 20260
September 20261
October 20260