Skip to content

Paltop 56-70014

by Paltop Advanced Dental Solutions Inc.

Paltop 56-70014 is a Class I device made by Paltop Advanced Dental Solutions Inc., listed in FDA GUDID since 30 Nov 2016 (UDI-DI 07290108691382), 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 Number07290108691382 UDI-DI Date30 Nov 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  • Withdrawn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
Paltop
Generic name
Dental implant abutment analog, laboratory
Model / Ref / Catalog
56-70014
Primary DI / UDI-DI
07290108691382
FDA product code
NDP
GMDN term
Dental implant abutment analog, laboratory
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Paltop Advanced Dental Solutions Inc.

See all devices from Paltop Advanced Dental Solutions Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)