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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 25 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9000645	FDA UDI	Class I	Active
Implant Prosthetics	9005032-50	FDA UDI	Class II	Unknown
Implant Prosthetics	9001203-25	FDA UDI	Class I	Unknown
Straumann	8001421	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007035	FDA UDI	Class II	Active
Implant Prosthetics	8000961	FDA UDI	Class II	Unknown
Implant Prosthetics	9002132-100	FDA UDI	Class II	Unknown
Implant Prosthetics	8000570	FDA UDI	Class II	Active
Preat	9000262	FDA UDI	Class II	Active
Preat	0802893	FDA UDI	Class II	Active
Implant Prosthetics	8001576	FDA UDI	Class II	Active
Preat	9003704	FDA UDI	Class I	Active
Preat Implant Prosthetics	9001567-F	FDA UDI	Class II	Active
Implant Prosthetics	9005535-10	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000080	FDA UDI	Class I	Active
Implant Prosthetics	9003731	FDA UDI	Class II	Unknown
Preat	9005790	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006703	FDA UDI	Class I	Active
Implant Prosthetics	9001254	FDA UDI	Class II	Active
Preat	9002235	FDA UDI	Class II	Active
Implant Prosthetics	8000475	FDA UDI	Class II	Active
O-Ring	1500602	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600403	FDA UDI	Class II	Active
Sphero Attachment	0812001	FDA UDI	Class II	Active
Implant Prosthetics	9003731-25	FDA UDI	Class II	Unknown
O-Ring	1800000	FDA UDI	Class II	Active
Hader Bar	0101720	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006775	FDA UDI	Class II	Active
Preat	8004815	FDA UDI	Class I	Active
Preat	0803792	FDA UDI	Class II	Active
Shiner Magnet System	1429683	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1705905C	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601502	FDA UDI	Class II	Active
Preat	9003752	FDA UDI	Class II	Active
Preat	3X691B0	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005778	FDA UDI	Class II	Active
Preat	0819768	FDA UDI	Class II	Active
Implant Prosthetics	9000854	FDA UDI	Class II	Active
Preat	2148172	FDA UDI	Class II	Active
Preat	0818774	FDA UDI	Class II	Active
Implant Prosthetics	9000135-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8001650	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601505	FDA UDI	Class II	Active
Shiner Magnet System	1400015	FDA UDI	Class I	Unknown
Implant Prosthetics	9002000-10	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600302	FDA UDI	Class II	Active
Implant Prosthetics	9005000-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9003732	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1607101C	FDA UDI	Class II	Active
Implant Prosthetics	9000475	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.