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
K972633Substantially Equivalent

Ultracell Suction Sponge

Ultracell Medical Technologies, Inc., North Stonington CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972633 is the FDA 510(k) clearance record for ULTRACELL SUCTION SPONGE, a class II device, cleared for Ultracell Medical Technologies, Inc. on under FDA product code HOZ (Sponge, Ophthalmic). FDA records list 24 510(k) clearances for Ultracell Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K972633.

Clearance record

Decision date
Received
(156 days to decision)
Product code
HOZ Sponge, Ophthalmic
Regulation
21 CFR 886.4790
Device class
Class II
Review panel
Ophthalmic
Applicant
Ultracell Medical Technologies, Inc. 183 Providence,, North Stonington CT
510(k) summary
Statement
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