RegWardenFDA facility compliance records
Facility

PALTOP ADVANCED DENTAL SOLUTIONS LTD

3 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2019: 2 recalls; 2021: 1 recalls201720182201920201202120222023202420252026
  • Recalls (3)

Devices registered here (2)

Recalls & enforcement

  • Class IITerminated2021-07-26
    Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head and titanium base, and an incongruence between the size engraved on the peek has been identified. Deviations may delay the final restoration.
  • Class IITerminated2019-11-18
    Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The Standard Platform Cover Screw will not fit in the Narrow Platform implant.
  • Class IITerminated2019-05-30
    Surface micro/nano topography on some of the implants contained within this lot may not be consistently present over the entire surface of the implant.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “PALTOP ADVANCED DENTAL SOLUTIONS LTD (FEI 3009161350) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009161350-paltop-advanced-dental-solutions-ltd/

Not open yet

Alerts for PALTOP ADVANCED DENTAL SOLUTIONS LTD

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.