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
K151748Substantially Equivalent

Clean & More

3M Deutschland GmbH, Seefeld, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151748 is the FDA 510(k) clearance record for Clean & More, a class II device, cleared for 3M Deutschland GmbH on under FDA product code PIP (Prophy Powder, Airbrush Accessory). FDA's definition for product code PIP reads: "An air polishing powder to be used with an airbrush for prophylaxis in the oral cavity". FDA records list 12 510(k) clearances for 3M Deutschland GmbH, from to . As of , FDA records show no recalls naming K151748.

Clearance record

Decision date
Received
(256 days to decision)
Product code
PIP Prophy Powder, Airbrush Accessory
Regulation
21 CFR 872.6080
Device class
Class II
Review panel
Dental
Applicant
3M Deutschland GmbH Espe Platz, Seefeld, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PIP

Trailing 12 months

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

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