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Coe® 250206

by Gc America Inc. 2 variants

Coe® 250206 is a Class I device made by Gc America Inc., listed in FDA GUDID since 20 Apr 2023 (UDI-DI 20386040012765), 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 Number20386040012765 UDI-DI Date20 Apr 2023ListedStatusListed 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  • Withdrawn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
Coe®
Generic name
Dental impression tray, single-use
Model / Ref / Catalog
250206
Primary DI / UDI-DI
20386040012765
FDA product code
EBH
GMDN term
Dental impression tray, single-use
Device class
Class I
Regulation number
872.3670
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental impression tray, single-use

Similar devices in this category

Other devices filed under Dental impression tray, single-use.

Other devices from Gc America Inc.

See all devices from Gc America Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)