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Inclusive 70-1052-COM0020

by Prismatik Dentalcraft, Inc.

Inclusive 70-1052-COM0020 is a Class II device made by Prismatik Dentalcraft, Inc., listed in FDA GUDID since 24 Oct 2015 (UDI-DI D745701052COM00200), registry data as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD745701052COM00200 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Inclusive
Generic name
Dental prosthesis/implant abutment screw
Model / Ref / Catalog
70-1052-COM0020
Primary DI / UDI-DI
D745701052COM00200
FDA product code
NHA
GMDN term
Dental prosthesis/implant abutment screw
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Height — 7.9 Millimeter

Related devices

Category: Dental prosthesis/implant abutment screw

Similar devices in this category

Other devices filed under Dental prosthesis/implant abutment screw.

Other devices from Prismatik Dentalcraft, Inc.

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Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)