510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862315Substantially Equivalent

Fyodorov Collagen Corneal Shield

Medical Technology Development Corp., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862315 is the FDA 510(k) clearance record for FYODOROV COLLAGEN CORNEAL SHIELD, a class I device, cleared for Medical Technology Development Corp. on under FDA product code MOE (Collagen Corneal Shield). FDA records list 5 510(k) clearances for Medical Technology Development Corp., from to . As of , FDA records show no recalls naming K862315.

Clearance record

Decision date
Received
(203 days to decision)
Product code
MOE Collagen Corneal Shield
Regulation
21 CFR 886.4750
Device class
Class I
Review panel
Ophthalmic
Applicant
Medical Technology Development Corp. 11300 49th St. N., Clearwater FL
Third party review
No

Clearances, product code MOE

Trailing 12 months

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

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