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Impress-Rite Imp-9007

by Crown Delta Corp.

Impress-Rite Imp-9007 is a Class II device made by Crown Delta Corp., listed in FDA GUDID since 5 Jul 2017 (UDI-DI 00818524020264), 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 Number00818524020264 UDI-DI Date5 Jul 2017ListedStatusListed 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  • Withdrawn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
Impress-Rite
Generic name
Silicone dental impression material
Model / Ref / Catalog
IMP-9007
Primary DI / UDI-DI
00818524020264
FDA product code
ELW
GMDN term
Silicone dental impression material
Device class
Class II
Regulation number
872.3660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Silicone dental impression material

Similar devices in this category

Other devices filed under Silicone dental impression material.

Other devices from Crown Delta Corp.

See all devices from Crown Delta Corp. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)