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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 28 of 80

Device	Model / Reference	Registries	Class	Status
Preat	710163	FDA UDI	Class II	Active
3i Certain	8001841	FDA UDI	Class I	Active
Sphero Block	0803300	FDA UDI	Class II	Active
Implant Prosthetics	8004761	FDA UDI	Class II	Active
Preat	0813795	FDA UDI	Class II	Active
Camlog	8003640	FDA UDI	Class I	Unknown
Equator	2149502	FDA UDI	Class II	Active
Preat	9002265-F	FDA UDI	Class II	Active
Implant Prosthetics	9007032-100	FDA UDI	Class II	Unknown
Implant Prosthetics	8000885	FDA UDI	Class II	Active
Ankylos	8004800	FDA UDI	Class I	Active
Hader	0101752	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007178	FDA UDI	Class II	Active
Implant Prosthetics	8000671	FDA UDI	Class II	Active
Implant Prosthetics	9001250	FDA UDI	Class II	Unknown
Fiber Technology	7009005	FDA UDI	Class II	Unknown
Implant Prosthetics	9000403	FDA UDI	Class I	Active
Implant Prosthetics	8004481	FDA UDI	Class I	Active
Preat	2148173	FDA UDI	Class II	Active
Preat	9000159	FDA UDI	Class II	Active
Sphero Attachments	0819034	FDA UDI	Class II	Active
Preci-Clix	01004TI	FDA UDI	Class I	Active
Preat	9000865-F	FDA UDI	Class II	Active
Implant Prosthetics	9005732-10	FDA UDI	Class II	Unknown
Preat Implant Driver Tools	9000062	FDA UDI	Class I	Active
Implant Prosthetics	8005186	FDA UDI	Class II	Active
Implant Prosthetics	9001475	FDA UDI	Class II	Active
O-Ring	1500606-2	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600200C	FDA UDI	Class II	Active
Sphero Attachment	0802102	FDA UDI	Class II	Active
Implant Prosthetics	8004488	FDA UDI	Class I	Active
Implant Prosthetics	8004872	FDA UDI	Class II	Active
Preci-Vertix	0101810	FDA UDI	Class I	Active
Preat	710224	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600106C	FDA UDI	Class II	Active
Implant Prosthetics	8003381	FDA UDI	Class II	Active
Preat	9000595	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006821	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600203C	FDA UDI	Class II	Active
Preat	1500195	FDA UDI	Class I	Active
Preat	9005659	FDA UDI	Class II	Active
Preat	0808634	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705706C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007122	FDA UDI	Class II	Active
Sphero Attachments	0819672	FDA UDI	Class II	Active
Camlog	8003330	FDA UDI	Class II	Active
Preat	1911702	FDA UDI	Class I	Unknown
Preat	0800152	FDA UDI	Class I	Active
Preat Implant Prosthetics	1600552	FDA UDI	Class II	Active
Sphero Attachment	0809117	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.