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A-dec 8000B

by A-Dec, Inc.

A-dec 8000B is a Class I device made by A-Dec, Inc., listed in FDA GUDID since 10 Nov 2022 (UDI-DI 10194665000202), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10194665000202 UDI-DI Date10 Nov 2022ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
A-dec
Generic name
Dental chair, electric
Model / Ref / Catalog
8000B, 8000
Primary DI / UDI-DI
10194665000202
FDA product code
NRU
GMDN term
Dental chair, electric
Device class
Class I
Regulation number
872.6250
GUDID distribution status
Not in Commercial Distribution

Other devices from A-Dec, Inc.

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  • A-dec 54.1074.01

    Class I

  • A-dec 54.1073.01

    Class I

See all devices from A-Dec, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)