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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 43 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9002175	FDA UDI	Class II	Active
Implant Prosthetics	9003738	FDA UDI	Class II	Unknown
Preat	710152	FDA UDI	Class II	Active
Preat	710052	FDA UDI	Class II	Active
Preat	9001269	FDA UDI	Class II	Active
Preat	710124	FDA UDI	Class II	Active
Preat	9000165	FDA UDI	Class II	Active
Preat	9000890	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006823	FDA UDI	Class II	Active
Preat Implant Prosthetics	1704702C	FDA UDI	Class II	Active
Implant Prosthetics	9001000-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9000532	FDA UDI	Class I	Unknown
Implant Prosthetics	9000910-10	FDA UDI	Class I	Unknown
Preat	7551440	FDA UDI	Class I	Unknown
Implant Prosthetics	9003750	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005801	FDA UDI	Class I	Active
Implant Prosthetics	9000200-25	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006467	FDA UDI	Class II	Active
Preat Implant Prosthetics	1602102	FDA UDI	Class II	Active
Nobel	8000715	FDA UDI	Class I	Active
Preci-Clix	0101280	FDA UDI	Class I	Active
Preat	7551220	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9003709	FDA UDI	Class I	Active
Implant Prosthetics	9004427	FDA UDI	Class II	Active
Implant Prosthetics	8000150	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600801	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004724	FDA UDI	Class II	Active
Equator	2144434	FDA UDI	Class II	Active
Preat	7551730	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007267-F	FDA UDI	Class II	Active
Sphero Attachments	0809925	FDA UDI	Class II	Active
CAMLOG® Screw-Line-compatible	8003641	FDA UDI	Class I	Active
Preat	3694CL0	FDA UDI	Class I	Active
Sphero Attachments	0819702	FDA UDI	Class II	Active
Preci 52	0101564	FDA UDI	Class I	Active
Sphero Attachments	0819033	FDA UDI	Class II	Active
Hader	0101753	FDA UDI	Class I	Active
Preat Implant Driver Tools	9000041	FDA UDI	Class I	Active
Implant Prosthetics	8004750	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600603C	FDA UDI	Class II	Active
Camlog	8003500	FDA UDI	Class I	Active
Legacy	9005600	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004752	FDA UDI	Class I	Active
Preat	9005162	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606702C	FDA UDI	Class II	Active
Implant Prosthetics	9004732-10	FDA UDI	Class II	Unknown
NobelBiocare™	8000530	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007030	FDA UDI	Class II	Active
Preat	3TL0H16	FDA UDI	Class I	Active
Camlog	8003215	FDA UDI	Class I	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.