A-Dec, Inc.

United StatesFDA applicant, unverified FDA FEI 3015729

A-Dec, Inc. is a medical device manufacturer, with 342 devices listed in FDA GUDID and FDA 510(k) (FDA Class I and II) and 1 FDA recall as of 12 Nov 2026.

Devices: 342
Registrations: FDA
FDA recalls: 1

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries: FDA GUDID 273
FDA 510(k) 69

A device listed in two registries counts in both.
Device classes: FDA Class I 336
FDA Class II 6
FDA recalls: 1 recall matched by name
Identifiers: FDA FEI 3015729
DUNS 009617473

At a glance

Counted by deviCERTS from registry records

Market reach

United States: FDA FEI, FDA recalls

What A-Dec, Inc. makes

A-Dec, Inc. manufactures dental delivery systems, dental suction systems, dental surgical power tool motors (electric), LED dental lights (line-powered), dental delivery system irrigation handpieces, medical device air compressors, electric dental chairs, and remotely-driven surgical/dental system drive cables.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue342

Newest first, rows 1-50 of 342

Search and filter all 342 devices

Rows 1-50 of 342

Showing 1-50 of 342

Company details

FDA FEI number: 3015729
DUNS number: 009617473
Address: 2601 Crestview Drive, Newberg, OR, 97132
Email: regulatory@a-dec.com
Phone: 5035389471

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by A-Dec, Inc., initiated on 2009-04-01. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

2009
- 1 Apr 2009 Z-0541-2011 Unclassified (pre-2012) Terminated The design of the Decade Plus 1221 chair backrest creates a possible pinch-point between the chair backrest and the underside of the armrests. Distribution: Worldwide distribution: US and Canada. Submission number: K913535

Frequently asked questions

How many devices does A-Dec, Inc. have in the registry?

The registry currently lists 342 devices for A-Dec, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list A-Dec, Inc.'s devices?

Among its 50 most recently registered devices, A-Dec, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do A-Dec, Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for A-Dec, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for A-Dec, Inc.?

FDA recall records list 1 recall initiated by A-Dec, Inc., the most recent initiated on 1 Apr 2009. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from A-Dec, Inc. in the registry?

The most recently registered devices listed for A-Dec, Inc. include A-dec 54.1073.00, A-dec 54.0924.01, A-dec 54.1074.01 and A-dec 54.1073.01.

Generated automatically from registry data and not verified by a human reviewer.