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Stabiliner CD001

by Crown Delta Corp.

Stabiliner CD001 is a Class II device made by Crown Delta Corp., listed in FDA GUDID since 3 Oct 2016 (UDI-DI 00866738000206), 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 Number00866738000206 UDI-DI Date3 Oct 2016ListedStatusListed 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  • Withdrawn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
Stabiliner
Generic name
Dental composite resin
Model / Ref / Catalog
CD001
Primary DI / UDI-DI
00866738000206
FDA product code
EMA
GMDN term
Dental composite resin
Device class
Class II
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 5 Milliliter

Related devices

Category: Dental composite resin

Similar devices in this category

Other devices filed under Dental composite resin.

Other devices from Crown Delta Corp.

See all devices from Crown Delta Corp. →

Properties

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