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
K944713Substantially Equivalent

W&h Micro Air Motor Lt25

A-dec, Inc., Newberg OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K944713 is the FDA 510(k) clearance record for W&H MICRO AIR MOTOR LT25, a class I device, cleared for A-Dec, Inc. on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list 69 510(k) clearances for A-Dec, Inc., from to . As of , FDA records show no recalls naming K944713.

Clearance record

Decision date
Received
(339 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
A-Dec, Inc. 2601 Crestview Dr., Newberg OR
510(k) summary
Statement
Third party review
No

Clearances, product code EFB

Trailing 12 months
3 clearances under product code EFB in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EFB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260