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DCI Edge C5552

by DCI International, LLC

DCI Edge C5552 is a Class I device made by DCI International, LLC, listed in FDA GUDID since 13 May 2024 (UDI-DI 00810021435527), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810021435527 UDI-DI Date13 May 2024ListedStatusListed 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  • Withdrawn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
DCI Edge
Generic name
Dental chair, electric
Model / Ref / Catalog
C5552
Primary DI / UDI-DI
00810021435527
FDA product code
NRU
GMDN term
Dental chair, electric
Device class
Class I
Regulation number
872.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental chair, electric

Other devices from DCI International, LLC

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    Class I

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    Class I

  • DCI Edge PJT600

    Class I

  • DCI Edge PJT601

    Class I

See all devices from DCI International, LLC →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)