510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860979Substantially Equivalent

Donaldson Natural Eyepatch

Keeler Instruments, Inc., Broomall PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860979 is the FDA 510(k) clearance record for DONALDSON NATURAL EYEPATCH, a class I device, cleared for Keeler Instruments, Inc. on under FDA product code HMP (Pad, Eye). FDA records list 60 510(k) clearances for Keeler Instruments, Inc., from to . As of , FDA records show no recalls naming K860979.

Clearance record

Decision date
Received
(21 days to decision)
Product code
HMP Pad, Eye
Regulation
21 CFR 878.4440
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Keeler Instruments, Inc. 456 Pkwy., Broomall PA
Third party review
No

Clearances, product code HMP

Trailing 12 months

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

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