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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 17 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9005130	FDA UDI	Class II	Active
Implant Prosthetics	9000603-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9001450-10	FDA UDI	Class I	Unknown
Equator	2149106	FDA UDI	Class II	Active
Implant Prosthetics	8000276	FDA UDI	Class II	Active
Implant Prosthetics	9001400-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006467-F	FDA UDI	Class II	Active
Implant Prosthetics	9001800-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000762	FDA UDI	Class II	Active
Preat Implant Prosthetics	9003736	FDA UDI	Class II	Active
Implant Prosthetics	8001061	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005975	FDA UDI	Class II	Active
Preat	710011	FDA UDI	Class II	Active
Preci-Sagix	0101306	FDA UDI	Class I	Active
Preat	9001965-F	FDA UDI	Class II	Active
Equator	2148175	FDA UDI	Class II	Active
Preat	0808633	FDA UDI	Class II	Active
Preat	710122	FDA UDI	Class II	Active
Preat	2RT0H10	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005761	FDA UDI	Class II	Active
Implant Prosthetics	9003763	FDA UDI	Class II	Active
Preat	9000190	FDA UDI	Class II	Active
Preat	0800168	FDA UDI	Class I	Unknown
Astra	8006630	FDA UDI	Class II	Active
Hader	0101702	FDA UDI	Class I	Active
Implant Prosthetics	8001476	FDA UDI	Class II	Active
Preat	9004165	FDA UDI	Class II	Active
Preat	2140CET	FDA UDI	Class I	Active
Implant Prosthetics	9001410-10	FDA UDI	Class I	Unknown
MegaGen	8004415	FDA UDI	Class I	Active
Preat	9007565	FDA UDI	Class II	Active
Preat	3724C20	FDA UDI	Class I	Active
Implant Prosthetics	9004483	FDA UDI	Class II	Active
Implant Prosthetics	8003483	FDA UDI	Class II	Active
Astra	8002030	FDA UDI	Class II	Active
O-Ring	9000010	FDA UDI	Class I	Active
Preat	2148199	FDA UDI	Class II	Active
Equator	2142075	FDA UDI	Class II	Active
Preat	0102004	FDA UDI	Class I	Unknown
Preat	9000564	FDA UDI	Class II	Active
Implant Prosthetics	9000476	FDA UDI	Class II	Active
Preat	9004935	FDA UDI	Class II	Active
Implant Prosthetics	8001871	FDA UDI	Class II	Active
Implant Prosthetics	8001250-10	FDA UDI	Class II	Unknown
Preat	9004765-F	FDA UDI	Class II	Active
Preat	0101372-2	FDA UDI	Class I	Active
Sphero Attachments	0803083	FDA UDI	Class II	Active
Implant Prosthetics	8004858	FDA UDI	Class II	Active
Preat	9001463	FDA UDI	Class II	Active
Implant Prosthetics	9005135-10	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.