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
K925064Substantially Equivalent for Some Indications

Relax-O-Guard

Aquatemp Service Co., Inc., Morristown NJ / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K925064 is the FDA 510(k) clearance record for RELAX-O-GUARD, a class I device, cleared for Aquatemp Service Co., Inc. on under FDA product code KMY (Positioner, Tooth, Preformed). FDA records list one 510(k) clearance for Aquatemp Service Co., Inc. As of , FDA records show no recalls naming K925064.

Clearance record

Decision date
Received
(342 days to decision)
Product code
KMY Positioner, Tooth, Preformed
Regulation
21 CFR 872.5525
Device class
Class I
Review panel
Dental
Applicant
Aquatemp Service Co., Inc. 58-C S. St., Morristown NJ
Third party review
No

Clearances, product code KMY

Trailing 12 months

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

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