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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 39 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9005732-50	FDA UDI	Class II	Unknown
Implant Prosthetics	8001089	FDA UDI	Class II	Active
Implant Prosthetics	9001781	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605904C	FDA UDI	Class II	Active
Preat Implant Prosthetics	8003440	FDA UDI	Class I	Unknown
Preat	0806906	FDA UDI	Class II	Active
Preat	3X691AP	FDA UDI	Class I	Active
O-Ring	1700554	FDA UDI	Class II	Active
Preat	0808610	FDA UDI	Class I	Active
Implant Prosthetics	8000120	FDA UDI	Class II	Active
Fiber Technology	7009004	FDA UDI	Class II	Unknown
Preat	1600034	FDA UDI	Class I	Active
Implant Prosthetics	9000275	FDA UDI	Class II	Active
Preat	8005010	FDA UDI	Class I	Active
Sphero Block	0806904	FDA UDI	Class II	Active
Nobel	8000790	FDA UDI	Class I	Unknown
Implant Prosthetics	9003700-25	FDA UDI	Class I	Unknown
Sphero Attachment	0812003	FDA UDI	Class II	Active
Implant Prosthetics	8003477	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600571	FDA UDI	Class II	Unknown
Preat	0817659	FDA UDI	Class II	Active
Shiner Magnet System	1429630	FDA UDI	Class II	Active
Preat Implant Prosthetics	1500150P	FDA UDI	Class I	Active
Preat	3TL0H13	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006763	FDA UDI	Class II	Active
Preat	9005453	FDA UDI	Class II	Active
Preat	9005467	FDA UDI	Class II	Active
Implant Prosthetics	9005932-10	FDA UDI	Class II	Unknown
Preat	0803403	FDA UDI	Class II	Active
Straumann	8001451	FDA UDI	Class I	Unknown
Implant Prosthetics	8004877	FDA UDI	Class II	Active
O-Ring	1700502	FDA UDI	Class II	Active
Preat	9006465	FDA UDI	Class II	Active
Preat	2RQ0091	FDA UDI	Class I	Unknown
Fiber Technology	7009070	FDA UDI	Class II	Unknown
Implant Prosthetics	8004489	FDA UDI	Class II	Active
Preat	0101301	FDA UDI	Class I	Unknown
Implant Prosthetics	9004429	FDA UDI	Class II	Active
Implant Prosthetics	9000276	FDA UDI	Class II	Active
Sphero Attachment	0811001	FDA UDI	Class II	Active
Implantlink Temporary Implant Cement	0907500	FDA UDI	Class II	Unknown
Implant Prosthetics	8000759	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007064	FDA UDI	Class II	Active
Implant Prosthetics	9003705-4	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1600825C	FDA UDI	Class II	Active
Implant Prosthetics	9001959	FDA UDI	Class II	Active
Implant Prosthetics	9006600-25	FDA UDI	Class I	Unknown
Preat	0819703	FDA UDI	Class II	Active
Implant Prosthetics	8005062	FDA UDI	Class II	Active
Preat	9000853	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.