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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 52 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9000663	FDA UDI	Class II	Active
Preat	2142904	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006759	FDA UDI	Class II	Active
Preat	9001695	FDA UDI	Class II	Active
Preci-Bar	0101163	FDA UDI	Class I	Active
Hiossen	8005119	FDA UDI	Class II	Active
Preat	9000963	FDA UDI	Class II	Active
Implant Prosthetics	9002100	FDA UDI	Class I	Active
Preat	7551350	FDA UDI	Class I	Unknown
Implant Prosthetics	8003659	FDA UDI	Class II	Active
Implant Prosthetics	8000861	FDA UDI	Class II	Unknown
Preci-Sagix	0101316-6	FDA UDI	Class I	Unknown
Preat	0813794	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007059	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605201C	FDA UDI	Class I	Unknown
Implant Prosthetics	8004458	FDA UDI	Class I	Active
Implant Prosthetics	9006800	FDA UDI	Class I	Active
Camlog	8003630	FDA UDI	Class II	Active
Preat	1911832	FDA UDI	Class I	Unknown
Preat	0819767	FDA UDI	Class II	Active
O-Ring	8005459	FDA UDI	Class II	Active
Sphero Attachment	0813077	FDA UDI	Class II	Active
Preat	2R195TI	FDA UDI	Class I	Active
Equator	2142897	FDA UDI	Class II	Active
Sphero Attachments	0812005	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605403	FDA UDI	Class II	Active
Implant Prosthetics	9002176	FDA UDI	Class II	Active
Implant Prosthetics	9005181	FDA UDI	Class II	Active
Implant Prosthetics	8002070	FDA UDI	Class II	Active
Preat	30861TI	FDA UDI	Class I	Active
O-Ring	1700574	FDA UDI	Class II	Active
Preat	3TL03H1	FDA UDI	Class I	Unknown
Preat	2142793	FDA UDI	Class II	Active
Preat	0101381	FDA UDI	Class I	Active
O-Ring Implant Abutments	1600814C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007221	FDA UDI	Class II	Active
Sphero Attachments	0811003	FDA UDI	Class II	Active
O-Ring	1600826	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608006	FDA UDI	Class II	Active
Preat	710671	FDA UDI	Class II	Active
Implant Prosthetics	9001251	FDA UDI	Class I	Active
Preat	0808737	FDA UDI	Class II	Active
Shiner Magnet System	1400005	FDA UDI	Class I	Unknown
Preat	9001595	FDA UDI	Class II	Active
Preat	7551610	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1706601C	FDA UDI	Class II	Active
Preat	9005230	FDA UDI	Class II	Active
Preat	710014	FDA UDI	Class II	Active
Preat	3X6AKS2	FDA UDI	Class I	Active
Preat Implant Prosthetics	1706602C	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.