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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 9 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9004663	FDA UDI	Class II	Active
Itl	8000067	FDA UDI	Class I	Active
Implant Prosthetics	8003473	FDA UDI	Class II	Active
Implant Prosthetics	9000232-100	FDA UDI	Class I	Unknown
Equator	2148176	FDA UDI	Class II	Active
Equator	2144442	FDA UDI	Class II	Active
Zest	4073261	FDA UDI	Class I	Active
Implant Prosthetics	9002050	FDA UDI	Class II	Active
Implant Prosthetics	9000235-10	FDA UDI	Class I	Unknown
Sphero Attachments	0809958	FDA UDI	Class II	Active
Preci-Clix	0101240	FDA UDI	Class I	Active
Implant Prosthetics	8002175	FDA UDI	Class II	Active
Astra®-compatible	8002100	FDA UDI	Class I	Active
Preat	9005063	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000073	FDA UDI	Class I	Active
Preat	9001765	FDA UDI	Class II	Active
Preat	1500632	FDA UDI	Class I	Active
Preat	7551700	FDA UDI	Class I	Unknown
Preat	9000864	FDA UDI	Class II	Active
Implant Prosthetics	9002177	FDA UDI	Class II	Active
Preat	710042	FDA UDI	Class II	Active
3i Certain	8001935	FDA UDI	Class II	Active
Preat	710652	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006801	FDA UDI	Class I	Active
Preat	9001835	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006689	FDA UDI	Class II	Active
Preat Implant Prosthetics	1607003C	FDA UDI	Class II	Active
Implant Prosthetics	9000832-50	FDA UDI	Class I	Unknown
O-Ring	1500530	FDA UDI	Class I	Active
Implant Prosthetics	9003736	FDA UDI	Class II	Unknown
Implant Prosthetics	8003571	FDA UDI	Class II	Active
Implant Prosthetics	8002161	FDA UDI	Class II	Active
Implant Prosthetics	9004426	FDA UDI	Class II	Active
Implant Prosthetics	9000176	FDA UDI	Class II	Active
Preat	0802796	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006830	FDA UDI	Class II	Active
Implant Prosthetics	9003754	FDA UDI	Class II	Active
Sphero Attachments	0818652	FDA UDI	Class II	Active
Preci-Sagix	0101362-6	FDA UDI	Class I	Unknown
Implant Prosthetics	9000400-10	FDA UDI	Class I	Unknown
Shiner Magnet System	1400006	FDA UDI	Class I	Unknown
A. Titan	8000010	FDA UDI	Class I	Active
Implant Prosthetics	9000232-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8004873	FDA UDI	Class II	Active
Preat	0812896	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605602	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600826C	FDA UDI	Class II	Active
Sphero Attachment	0801405	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005964	FDA UDI	Class II	Active
Nobel	8000691	FDA UDI	Class I	Unknown

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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.