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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 7 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9006590	FDA UDI	Class II	Active
3i Certain	8001910	FDA UDI	Class I	Active
Preat	0800148	FDA UDI	Class I	Active
Preat	2141727	FDA UDI	Class II	Active
Implant Prosthetics	9005380	FDA UDI	Class II	Active
Implant Prosthetics	9000700	FDA UDI	Class I	Active
O-Ring	1700552	FDA UDI	Class II	Active
Implant Prosthetics	9000403-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8001562	FDA UDI	Class II	Unknown
Implant Prosthetics	9000850	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600502C	FDA UDI	Class II	Active
Sphero Attachments	0813911	FDA UDI	Class II	Active
Preat	1300360	FDA UDI	Class I	Unknown
Preat	0819686	FDA UDI	Class II	Active
Preat	1911733	FDA UDI	Class I	Unknown
Preat	2R700TI	FDA UDI	Class I	Active
Sphero Attachments	0800649	FDA UDI	Class II	Active
Preci-Bar	0101104	FDA UDI	Class I	Unknown
Preat	0101214	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1605901C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007067-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006704	FDA UDI	Class I	Active
Implant Prosthetics	8000950-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9003761	FDA UDI	Class II	Active
Preat	0819691	FDA UDI	Class II	Active
Astra	8006730	FDA UDI	Class II	Active
Implant Prosthetics	9005100	FDA UDI	Class I	Active
Shiner Magnet System	1429625	FDA UDI	Class II	Unknown
Preat	0802800	FDA UDI	Class II	Active
NobelBiocare™ Tri-Lobe-compatible	8000741	FDA UDI	Class I	Active
Preat Implant Prosthetics	9003739	FDA UDI	Class II	Active
Preci-Vertix	0101819	FDA UDI	Class I	Active
Preat	0101212	FDA UDI	Class I	Unknown
Implant Prosthetics	9002250	FDA UDI	Class II	Active
Preat Implant Prosthetics	1607104C	FDA UDI	Class II	Unknown
Implant Prosthetics	9000579	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600602	FDA UDI	Class II	Active
Implant Prosthetics	9000132	FDA UDI	Class I	Unknown
Preat	0101238	FDA UDI	Class I	Active
Preat	9000168	FDA UDI	Class II	Active
Implant Prosthetics	9003757-10	FDA UDI	Class II	Active
Implant Prosthetics	9001832-50	FDA UDI	Class II	Unknown
O-Ring	1700903	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600504C	FDA UDI	Class II	Active
Implant Prosthetics	8000283	FDA UDI	Class II	Active
Implant Prosthetics	9000432-100	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1600822C	FDA UDI	Class II	Active
Implant Prosthetics	8004878	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007180	FDA UDI	Class II	Active
Implant Prosthetics	9006632-10	FDA UDI	Class II	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.