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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 64 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9006532-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9003761	FDA UDI	Class II	Unknown
Implant Prosthetics	8000462	FDA UDI	Class II	Active
Preat	2RQ0031	FDA UDI	Class I	Active
Preat	0805054-4	FDA UDI	Class I	Active
Implant Prosthetics	9001832-10	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600816C	FDA UDI	Class II	Active
Preat	50005-20	FDA UDI	Class II	Unknown
Preat	9007051	FDA UDI	Class I	Active
Implant Prosthetics	8001062	FDA UDI	Class II	Active
Implant Prosthetics	9006632-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9000977	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000445	FDA UDI	Class I	Active
Implant Prosthetics	8004473	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000803	FDA UDI	Class I	Active
Preat	9008565-F	FDA UDI	Class II	Active
Preat	9001665-F	FDA UDI	Class II	Active
Preat	9000530	FDA UDI	Class II	Active
Implant Prosthetics	9005103-10	FDA UDI	Class I	Unknown
Preci Profile	0101400	FDA UDI	Class I	Unknown
Implant Prosthetics	9005451	FDA UDI	Class I	Active
Implant Prosthetics	9006400	FDA UDI	Class I	Active
Implant Prosthetics	8003380	FDA UDI	Class II	Active
Implant Prosthetics	8001471	FDA UDI	Class II	Active
Sphero Attachments	0809116	FDA UDI	Class II	Active
Preat	0804600	FDA UDI	Class I	Active
O-Ring	1700905	FDA UDI	Class II	Active
Preat	0112260	FDA UDI	Class I	Unknown
Preat	9001659	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007121	FDA UDI	Class II	Active
Straumann	8001341	FDA UDI	Class I	Active
O-Ring	1700402	FDA UDI	Class II	Active
Preat	50000-20P	FDA UDI	Class II	Unknown
Preat	710211	FDA UDI	Class II	Active
O-Ring Implant Abutments	1500244	FDA UDI	Class II	Unknown
Shiner Magnet System	1400251	FDA UDI	Class I	Unknown
Preat	9005995	FDA UDI	Class II	Active
Implant Prosthetics	9000632-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9000330	FDA UDI	Class II	Active
Sphero Block	0802539	FDA UDI	Class II	Active
Implant Prosthetics	9000489	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601503	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000076	FDA UDI	Class I	Active
Preat Implant Driver Tools	9000074	FDA UDI	Class I	Active
Implant Prosthetics	8004920	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600902	FDA UDI	Class II	Active
Preat	2142081	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007269	FDA UDI	Class II	Active
Preat	7551515	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006452	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.