Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
1 to 6 of 6 Results
510(K) Number: K220823
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction w... 2 07/08/2024 FEI # 2918719
Preat Corp
Neodent GM X 6mm Engaging Titanium Base, REF: 9007162 2 03/24/2023 FEI # 2918719
Preat Corp
Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental 2 10/24/2023 FEI # 2918719
Preat Corp
Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental 2 10/24/2023 FEI # 2918719
Preat Corp
Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only. ... 2 10/24/2023 FEI # 2918719
Preat Corp
Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx O... 2 07/10/2025 FEI # 2918719
Preat Corp
-
-