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Preat Corp

11 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662 recall (Z-2514-2025)Preat Corp2025-09-03
Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pa recall (Z-2107-2025)Preat Corp2025-07-10
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutment recall (Z-1987-2025)Preat Corp2025-06-18
Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digita recall (Z-2687-2024)Preat Corp2024-08-19
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjun recall (Z-2318-2024)Preat Corp2024-07-08
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 recall (Z-1321-2024)Preat Corp2024-03-20
Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Onl recall (Z-0152-2024)Preat Corp2023-10-24
Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Onl recall (Z-0153-2024)Preat Corp2023-10-24
Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single recall (Z-0154-2024)Preat Corp2023-10-24
Neodent GM X 6mm Engaging Titanium Base, REF: 9007162 recall (Z-1285-2023)Preat Corp2023-03-24
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in recall (Z-1226-2023)Preat Corp2023-03-06

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Every clearance here is in the API, with alerts when new ones post.