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ScanBox pro - Candid 001

by Dental Monitoring 3 variants

ScanBox pro - Candid 001 (1015-001) is a Class I device made by Dental Monitoring, listed in FDA GUDID since 14 Feb 2025 (UDI-DI 03760405340169), 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 Number03760405340169 UDI-DI Date14 Feb 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  • Withdrawn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
ScanBox pro - Candid
Generic name
Dental cheek retractor, professional, reusable
Model / Ref / Catalog
001, 1015-001
Primary DI / UDI-DI
03760405340169
FDA product code
EIG
GMDN term
Dental cheek retractor, professional, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental cheek retractor, professional, reusableDental cheek retractor, home-use

Similar devices

Other devices filed under FDA product code EIG (Retractor, All Types).

Other devices from Dental Monitoring

See all devices from Dental Monitoring →

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)