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Paltop 80-70003

by Paltop Advanced Dental Solutions Inc.

Paltop 80-70003 is a Class I device made by Paltop Advanced Dental Solutions Inc., listed in FDA GUDID since 2 Mar 2021 (UDI-DI 07290114690003), 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 Number07290114690003 UDI-DI Date2 Mar 2021ListedStatusListed 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  • Withdrawn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
Paltop
Generic name
Dental prosthesis/implant abutment screw analog, single-use
Model / Ref / Catalog
80-70003
Primary DI / UDI-DI
07290114690003
FDA product code
NDP
GMDN term
Dental prosthesis/implant abutment screw analog, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental prosthesis/implant abutment screw analog, single-use

Other devices from Paltop Advanced Dental Solutions Inc.

See all devices from Paltop Advanced Dental Solutions Inc. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)