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A-dec 511FLT

by A-Dec, Inc.

A-dec 511FLT is a Class I device made by A-Dec, Inc., listed in FDA GUDID since 19 May 2025 (UDI-DI 10194665006594), 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 Number10194665006594 UDI-DI Date19 May 2025ListedStatusListed 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  • Withdrawn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 chair, electric
Model / Ref / Catalog
511FLT
Primary DI / UDI-DI
10194665006594
FDA product code
NRU
GMDN term
Dental chair, electric
Device class
Class I
Regulation number
872.6250
GUDID distribution status
In Commercial Distribution

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)