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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 75 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9000151	FDA UDI	Class I	Active
Implant Prosthetics	8000886	FDA UDI	Class II	Active
Implant Prosthetics	9000100-25	FDA UDI	Class I	Unknown
Shiner Magnet System	1429665	FDA UDI	Class II	Unknown
Implant Prosthetics	9001489	FDA UDI	Class II	Active
Preci-Bar	0101165	FDA UDI	Class I	Active
Astra	8006540	FDA UDI	Class I	Unknown
Preat Implant Driver Tools	9000043	FDA UDI	Class I	Active
Implant Prosthetics	9003736-50	FDA UDI	Class II	Unknown
Implant Prosthetics	9000500-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000562	FDA UDI	Class II	Active
O-Ring	1800010	FDA UDI	Class I	Active
Sphero Attachments	0819663	FDA UDI	Class II	Active
Preci-Sagix	0101312-50	FDA UDI	Class I	Unknown
Implant Prosthetics	9005650	FDA UDI	Class II	Active
Implant Prosthetics	8004487	FDA UDI	Class I	Active
O-Ring	1701701	FDA UDI	Class II	Active
Implant Prosthetics	8001225	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004735	FDA UDI	Class II	Active
Implant Prosthetics	9002232-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	0600F13	FDA UDI	Class I	Active
NobelActive™/Conical-compatible	8004941	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006601	FDA UDI	Class I	Active
Equator	2142993	FDA UDI	Class II	Active
Implant Prosthetics	9001500-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9001680	FDA UDI	Class II	Active
Implant Prosthetics	8005176	FDA UDI	Class II	Active
Implant Prosthetics	8001570	FDA UDI	Class II	Active
Sphero Attachment	0810000	FDA UDI	Class II	Active
Shiner Magnet System	1400281	FDA UDI	Class I	Unknown
Sphero Attachments	0803077	FDA UDI	Class II	Active
Implant Prosthetics	9004479	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601504C	FDA UDI	Class II	Active
Implant Prosthetics	8001086	FDA UDI	Class II	Active
Sphero Attachments	0811730	FDA UDI	Class II	Active
Implant Prosthetics	8001220	FDA UDI	Class II	Active
O-Ring	1776003	FDA UDI	Class I	Active
O-Ring Implant Abutments	1500242	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600030	FDA UDI	Class I	Active
Itl	8000056	FDA UDI	Class I	Active
Equator	2142891	FDA UDI	Class II	Active
O-Ring	1700556	FDA UDI	Class II	Active
Implant Prosthetics	8004486	FDA UDI	Class I	Active
Implant Prosthetics	9002278	FDA UDI	Class II	Active
Implant Prosthetics	9001532-10	FDA UDI	Class II	Unknown
Equator	2142905	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001967-F	FDA UDI	Class II	Active
Implant Prosthetics	9005003-25	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006423	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006745	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.