FDA Device Intelligence
Home › A-DEC, INC. › A-dec

A-dec

A-DEC, INC. · Model 54.0882.00 · UDI-DI 10194665004538

EFA
1
510(k) clearances
265
Adverse events
3
Recalls
19
Facilities

Description

Electric HS Package,M25L,Master Matic,OTC

Recalls

DateFirmReason
2014-06-13Dental EZ Group Star Dental DivisionThe housing of 5K motor was laser marked incorrectly as a 20K motor. The recall was expanded in September 2014 to include additional lot #2251181.
2010-08-11Dental EZ Stardental DivisionThe housing of 5K motor is labeled as a 20K motor.
2006-12-01Stardental DivisionEnd cap component can disassemble.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.