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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 24 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9003731	FDA UDI	Class II	Active
Implant Prosthetics	9000164	FDA UDI	Class II	Unknown
Implant Prosthetics	9000180	FDA UDI	Class II	Active
Implant Prosthetics	8000971	FDA UDI	Class II	Active
Preat	0101232	FDA UDI	Class I	Active
Implant Prosthetics	8002272	FDA UDI	Class II	Active
Implant Prosthetics	9005100-10	FDA UDI	Class I	Unknown
Sphero Attachments	0802001	FDA UDI	Class II	Active
Zimmer	8000115	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005903	FDA UDI	Class I	Active
Implant Prosthetics	9001779	FDA UDI	Class II	Active
Implant Prosthetics	8003361	FDA UDI	Class II	Active
Astra	8002235	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605603C	FDA UDI	Class II	Active
Preat	9000967	FDA UDI	Class II	Active
Implant Prosthetics	9001654	FDA UDI	Class II	Active
Implant Prosthetics	8000220	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007169	FDA UDI	Class II	Active
Preat	9000862	FDA UDI	Class II	Active
Sphero Attachment	0801003	FDA UDI	Class II	Active
Preat	2142104	FDA UDI	Class II	Active
Implant Prosthetics	8001680	FDA UDI	Class II	Active
Zimmer	8000102	FDA UDI	Class I	Active
Implant Prosthetics	9001577	FDA UDI	Class II	Active
Preat	7551420	FDA UDI	Class I	Unknown
Implant Prosthetics	9000730-10	FDA UDI	Class II	Active
Preat	9005990	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600102	FDA UDI	Class II	Active
Preat Implant Prosthetics	8000060	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1602102C	FDA UDI	Class II	Active
Hiossen	8005004	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600101C	FDA UDI	Class II	Active
Implant Prosthetics	8004750-10	FDA UDI	Class II	Unknown
MegaGen AnyRidge®-compatible	8004435	FDA UDI	Class II	Active
Implant Prosthetics	8003250-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9000132-50	FDA UDI	Class II	Unknown
Implant Prosthetics	8001550-10	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600604C	FDA UDI	Class II	Active
Implant Prosthetics	9004403-25	FDA UDI	Class I	Unknown
Preat	9003743	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005922	FDA UDI	Class II	Active
Implant Prosthetics	9005175	FDA UDI	Class II	Active
Camlog	8003475	FDA UDI	Class II	Active
O-Ring	1705605	FDA UDI	Class II	Active
Implant Prosthetics	8002271	FDA UDI	Class II	Active
Sphero Attachments	0809433	FDA UDI	Class II	Active
Implant Prosthetics	8002162	FDA UDI	Class II	Active
Sphero Attachments	0813070	FDA UDI	Class II	Active
Preat	0819766	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005901	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.