Is this your brand? Sign in to claim ownership.
Sign in to claim this brandPREAT Corporation
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2625 Skyway Drive, Santa Maria, CA, 93455
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2918719
- DUNS Number
- —
Catalogue (3952)
Page 16 of 80| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| O-Ring | 1700503 | FDA UDI | Class II | Active |
| Implant Prosthetics | 8000972 | FDA UDI | Class II | Active |
| Preat | 710164 | FDA UDI | Class II | Active |
| Implant Prosthetics | 8003577 | FDA UDI | Class II | Active |
| Implant Prosthetics | 8005059 | FDA UDI | Class II | Active |
| Preat | 30295NP | FDA UDI | Class I | Active |
| Preat | 9000467 | FDA UDI | Class II | Active |
| Preat Implant Prosthetics | 9005945 | FDA UDI | Class I | Active |
| Preat | 0101277 | FDA UDI | Class I | Active |
| O-Ring | 1700551 | FDA UDI | Class II | Active |
| Sagix | 0101311 | FDA UDI | Class I | Active |
| Equator | 2148678 | FDA UDI | Class II | Active |
| O-Ring | 1702101 | FDA UDI | Class II | Active |
| Clix Ball Implant Abutments | 1608001 | FDA UDI | Class II | Active |
| Vertix | 0101840 | FDA UDI | Class I | Active |
| Implant Prosthetics | 9004419 | FDA UDI | Class II | Active |
| Implant Prosthetics | 8002925 | FDA UDI | Class II | Unknown |
| Camlog | 8003235 | FDA UDI | Class II | Active |
| 3i Certain | 8002800 | FDA UDI | Class I | Unknown |
| Astra | 8002051 | FDA UDI | Class I | Active |
| Preat | 9006695 | FDA UDI | Class II | Active |
| Preci-Sagix | 0101385 | FDA UDI | Class I | Active |
| Astra | 8006435 | FDA UDI | Class II | Active |
| Preat | 1400330 | FDA UDI | Class I | Unknown |
| Implant Prosthetics | 9000803 | FDA UDI | Class I | Unknown |
| Astra | 8006461 | FDA UDI | Class II | Active |
| Preat | 9001565 | FDA UDI | Class II | Active |
| Preat | 9005190 | FDA UDI | Class II | Active |
| Preat Implant Prosthetics | 9005904 | FDA UDI | Class I | Active |
| Preat | 7009041 | FDA UDI | Class I | Unknown |
| Sphero Block | 0802895 | FDA UDI | Class II | Active |
| Preat | 3ZX0150 | FDA UDI | Class I | Active |
| Preat | 01K1281 | FDA UDI | Class I | Active |
| Preat | 0803793 | FDA UDI | Class II | Active |
| Preat Implant Prosthetics | 9002003 | FDA UDI | Class I | Active |
| Preat | 06000F8 | FDA UDI | Class I | Active |
| Preat Implant Prosthetics | 9006489 | FDA UDI | Class II | Active |
| Preat | 710044 | FDA UDI | Class II | Active |
| Straumann | 8001482 | FDA UDI | Class II | Active |
| Implant Prosthetics | 8004485 | FDA UDI | Class I | Active |
| Preat | 9001576 | FDA UDI | Class II | Active |
| NobelBiocare™ Tri-Lobe-compatible | 8000400 | FDA UDI | Class I | Active |
| Sphero Attachment | 0800753 | FDA UDI | Class II | Active |
| O-Ring | 1776003-3 | FDA UDI | Class I | Unknown |
| Preat | 9000061 | FDA UDI | Class I | Active |
| Implant Prosthetics | 9005378 | FDA UDI | Class II | Active |
| Preat | 0101271C | FDA UDI | Class I | Active |
| Preat | 0102002 | FDA UDI | Class I | Active |
| Preat | 9001235 | FDA UDI | Class II | Active |
| Preat Implant Prosthetics | 9005003 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (11)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jun 25, 2025 | Z-2514-2025 | — | open, classified | Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, resulting in restoration delay. |
| Jun 24, 2025 | Z-2107-2025 | — | open, classified | Due to manufacturing error, digital analog rotational feature is 180 degrees off. |
| Apr 2, 2025 | Z-1987-2025 | — | open, classified | Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant. |
| Jun 25, 2024 | Z-2687-2024 | — | open, classified | Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations. |
| Apr 10, 2024 | Z-2318-2024 | — | open, classified | Due to incorrect milled titanium abutment being packaged and labeled. |
| Feb 9, 2024 | Z-1321-2024 | — | open, classified | Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant. |
| Jul 18, 2023 | Z-0153-2024 | — | open, classified | The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage |
| Jul 18, 2023 | Z-0152-2024 | — | open, classified | The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage |
| Jul 18, 2023 | Z-0154-2024 | — | open, classified | The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage |
| Feb 21, 2023 | Z-1285-2023 | — | open, classified | Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture, which could result in the abutment/screw/crown being ingested by the patient. |
| Feb 1, 2023 | Z-1226-2023 | — | open, classified | Product is labeled with an incorrect expiration date. |