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
K132796Substantially Equivalent

Suntouch Eye Spear

HuiZhou Foryou Medical Devices Co., Ltd., Shanghai, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132796 is the FDA 510(k) clearance record for SUNTOUCH EYE SPEAR, a class II device, cleared for Huizhou Foryou Medical Devices Co., Ltd. on under FDA product code HOZ (Sponge, Ophthalmic). FDA records list 22 510(k) clearances for Huizhou Foryou Medical Devices Co., Ltd., from to . As of , FDA records show no recalls naming K132796.

Clearance record

Decision date
Received
(54 days to decision)
Product code
HOZ Sponge, Ophthalmic
Regulation
21 CFR 886.4790
Device class
Class II
Review panel
Ophthalmic
Applicant
Huizhou Foryou Medical Devices Co., Ltd. P.O. Box 120-119, Shanghai, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HOZ

Trailing 12 months

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

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