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A-dec 363

by A-Dec, Inc.

A-dec 363 is a Class I device made by A-Dec, Inc., listed in FDA GUDID since 8 Nov 2022 (UDI-DI 10194665000127), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number10194665000127 UDI-DI Date8 Nov 2022ListedStatusListed GUDID: 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  • Withdrawn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 cuspidor
Model / Ref / Catalog
363
Primary DI / UDI-DI
10194665000127
FDA product code
EBR
GMDN term
Dental cuspidor
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental cuspidor

Similar devices

Also classified as Dental cuspidor.

Similar devices

Other devices filed under FDA product code EBR (Unit, Suction Operatory).

Other devices from A-Dec, Inc.

  • A-dec 54.1073.00

    Class I

  • A-dec 54.0924.01

    Class I

  • 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)