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Beesure BE504D

by Ascend Eagle Incorporated

Beesure BE504D is a Class I device made by Ascend Eagle Incorporated, listed in FDA GUDID since 23 May 2022 (UDI-DI 10817508021614), 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 Number10817508021614 UDI-DI Date23 May 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  • Withdrawn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
Beesure
Generic name
Denture repair kit, professional
Model / reference
BE504D
Description
Beesure Micro Applicators 400 /BX , Blue Regular
Primary DI / UDI-DI
10817508021614
FDA product code
EJB
GMDN term
Denture repair kit, professional
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Denture repair kit, professional

Similar devices

Other devices filed under FDA product code EJB (Handle, Instrument, Dental).

Other devices from Ascend Eagle Incorporated

See all devices from Ascend Eagle Incorporated →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)