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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 8 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9002100-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9000403-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8002289	FDA UDI	Class II	Active
Equator	2148741	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001703	FDA UDI	Class I	Active
Preat	9002153	FDA UDI	Class II	Active
Preat	9000767	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006668	FDA UDI	Class II	Active
Preat	0818653	FDA UDI	Class II	Active
Preat	0813083	FDA UDI	Class II	Active
Preat	710081	FDA UDI	Class II	Active
Preat	0811000	FDA UDI	Class II	Active
Implant Prosthetics	9001575	FDA UDI	Class II	Active
Implant Prosthetics	9001603-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9005100-25	FDA UDI	Class I	Unknown
Equator	2148537	FDA UDI	Class II	Active
Preat	710104	FDA UDI	Class II	Active
Implant Prosthetics	8000579	FDA UDI	Class II	Active
Implant Prosthetics	9001800	FDA UDI	Class I	Active
Implant Prosthetics	9000300-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8001477	FDA UDI	Class II	Active
Sphero Attachments	0809104	FDA UDI	Class II	Active
Implant Prosthetics	9002281	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005862	FDA UDI	Class II	Active
Preat	9001410	FDA UDI	Class I	Active
Preat Implant Driver Tools	9000064	FDA UDI	Class I	Active
Preat	9002130	FDA UDI	Class II	Active
Preat	9007290	FDA UDI	Class II	Active
Preat	710484	FDA UDI	Class II	Active
Preat	710482	FDA UDI	Class II	Active
Preat	0101355	FDA UDI	Class I	Unknown
Implant Prosthetics	9000735-10	FDA UDI	Class II	Active
Preat	9001965	FDA UDI	Class II	Active
Implant Prosthetics	9001232-10	FDA UDI	Class II	Unknown
Preat	9000635	FDA UDI	Class II	Active
Implant Prosthetics	9001621	FDA UDI	Class II	Unknown
Implant Prosthetics	9003753	FDA UDI	Class I	Active
Implant Prosthetics	9004489	FDA UDI	Class II	Active
Preat	0808635	FDA UDI	Class II	Active
Sphero Attachment	0819654	FDA UDI	Class II	Active
Preat	9005353	FDA UDI	Class II	Active
Preat	50000-20	FDA UDI	Class II	Unknown
Preat	2R100NP	FDA UDI	Class I	Active
Implant Prosthetics	8003475	FDA UDI	Class II	Unknown
Astra	8006551	FDA UDI	Class I	Active
Preat	7551520	FDA UDI	Class I	Unknown
Preat	9006795	FDA UDI	Class II	Active
Equator	2148117	FDA UDI	Class II	Active
Preat	0803811	FDA UDI	Class II	Active
Branemark	8001015	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.