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PREAT Corporation

Last updated September 17, 2026

Information

Country: US
Address: 2625 Skyway Drive, Santa Maria, CA, 93455
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2918719
DUNS Number: —

Catalogue (3952)

Page 35 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9001732-10	FDA UDI	Class II	Unknown
Preat	0101234	FDA UDI	Class I	Active
Preat	9001464	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600303C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007177	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007204	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005900	FDA UDI	Class I	Active
Preat	9003733-10	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605603	FDA UDI	Class II	Active
Preat	0800149	FDA UDI	Class I	Active
Preat	0812893	FDA UDI	Class II	Active
Implant Prosthetics	9004476	FDA UDI	Class II	Active
Implant Prosthetics	8004450	FDA UDI	Class I	Unknown
Shiner Magnet System	1429682	FDA UDI	Class II	Unknown
Implant Prosthetics	9000930-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9006400-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8003559	FDA UDI	Class II	Active
Preat	0800720	FDA UDI	Class I	Active
Preat	0813203	FDA UDI	Class II	Active
Implant Prosthetics	9000700-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9005830	FDA UDI	Class II	Unknown
Preat	2142803	FDA UDI	Class II	Active
Implant Prosthetics	8005150-25	FDA UDI	Class II	Unknown
O-Ring	1708005	FDA UDI	Class II	Active
Preat	0101281C	FDA UDI	Class I	Unknown
O-Ring	1700404	FDA UDI	Class II	Active
Sphero Attachments	0811006	FDA UDI	Class II	Active
Implant Prosthetics	9001651	FDA UDI	Class I	Active
Hader	0101754	FDA UDI	Class I	Active
Preat	8005115	FDA UDI	Class I	Active
Preat	0800704	FDA UDI	Class II	Active
O-Ring	1500530-4	FDA UDI	Class I	Unknown
O-Ring	1500502-4	FDA UDI	Class I	Unknown
Preat	0101219	FDA UDI	Class I	Unknown
Equator	2142076	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007068	FDA UDI	Class II	Active
Implant Prosthetics	9001232-50	FDA UDI	Class II	Unknown
Preat	9000359	FDA UDI	Class II	Active
Implant Prosthetics	8000876	FDA UDI	Class II	Active
Gingivamoll	0906411	FDA UDI	Class I	Unknown
Implant Prosthetics	9000477	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005930	FDA UDI	Class II	Active
Implant Prosthetics	8000720	FDA UDI	Class II	Active
Implant Prosthetics	9005278	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706503C	FDA UDI	Class II	Active
Preat	7551430	FDA UDI	Class I	Unknown
Preat	0800755	FDA UDI	Class II	Active
Preat	7551715	FDA UDI	Class I	Unknown
Implant Prosthetics	9000332	FDA UDI	Class I	Unknown
Preat	0803809	FDA UDI	Class II	Active

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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.