Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Paltop Advanced Dental Solutions with 8 device recalls and 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 2025: Paltop Dental Implant System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 29, 2025 | Paltop Dental Implant SystemK243983 · DZE | 510(k) clearances |
| May 22, 2024 | Paltop Short ImplantsK232740 · DZE | 510(k) clearances |
| May 25, 2022 | Paltop Conical Implant SystemK220200 · DZE | 510(k) clearances |
| Nov 30, 2021 | Paltop Narrow ImplantK210117 · DZE | 510(k) clearances |
| Jul 26, 2021 | Scan Abutment SP, Cat. No. 30-70101 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a dClass II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Jul 26, 2021 | Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a dClass II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Jul 26, 2021 | Scan Abutment WP, Cat. No. 30-70106 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a Class II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Jul 26, 2021 | Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a Class II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Jul 26, 2021 | Scan Abutment SU, Cat. No. 30-70104 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a Class II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Jul 26, 2021 | Scan Abutment PCA, Cat. No. 30-70105 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide aClass II · Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head | Device recalls |
| Nov 18, 2019 | Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020Class II · Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The S | Device recalls |
| May 30, 2019 | Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024PClass II · Surface micro/nano topography on some of the implants contained within this lot may not be consistently present over th | Device recalls |
| Aug 27, 2013 | PALTOP NARROW IMPLANT, PALTOP SHORT IMPLANTK130462 · DZE | 510(k) clearances |
| Aug 22, 2013 | PALTOP DENTAL IMPLANT - STERILE ACCESSORIESK131451 · DZE | 510(k) clearances |
| Apr 20, 2012 | PALTOP DENTAL IMPLANT SYSTEMK112795 · DZE | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
