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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 72 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9004400-25	FDA UDI	Class I	Unknown
Preat	9006565-F	FDA UDI	Class II	Active
Preat	9005261	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600200	FDA UDI	Class II	Active
Implant Prosthetics	8004462	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1500245	FDA UDI	Class II	Unknown
Sphero Attachment	0813072	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004730	FDA UDI	Class II	Active
Implant Prosthetics	9005130-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9003700-100	FDA UDI	Class I	Unknown
Sphero Block	0814503	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000066	FDA UDI	Class I	Active
Preat	9000869	FDA UDI	Class II	Active
Implant Prosthetics	9004730-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9001430	FDA UDI	Class II	Active
Preat	1500212	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005800	FDA UDI	Class I	Active
Implant Prosthetics	8001489	FDA UDI	Class II	Active
Implant Prosthetics	8000859	FDA UDI	Class II	Active
Preat	1700555	FDA UDI	Class II	Active
Shiner Magnet System	1429663	FDA UDI	Class II	Unknown
Preat	50000-35	FDA UDI	Class II	Unknown
Preat	9005164	FDA UDI	Class II	Active
Preat	0101293	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605405	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007077	FDA UDI	Class II	Active
Preat	9005890	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606401C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1707103C	FDA UDI	Class II	Active
Implant Prosthetics	8000571	FDA UDI	Class II	Active
Preat	9001467	FDA UDI	Class II	Active
Preat	7551810	FDA UDI	Class I	Unknown
Preat	2142092	FDA UDI	Class II	Active
Preat	0101322-2	FDA UDI	Class I	Active
Implant Prosthetics	9002132	FDA UDI	Class II	Unknown
Preat	0600F14	FDA UDI	Class I	Active
Preat	3694CL8	FDA UDI	Class I	Active
Implant Prosthetics	8004875	FDA UDI	Class II	Active
Sphero Attachments	0819671	FDA UDI	Class II	Active
Implant Prosthetics	9005559	FDA UDI	Class II	Active
Preat	9006553	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706703C	FDA UDI	Class II	Active
Preat	710093	FDA UDI	Class II	Active
Preat	710101	FDA UDI	Class II	Active
Preat	1500150	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605802C	FDA UDI	Class II	Active
Preat	0101224	FDA UDI	Class I	Active
Preat Implant Prosthetics	9003760-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9000632-100	FDA UDI	Class I	Unknown
Implant Prosthetics	8003459	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.