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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 56 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9000267	FDA UDI	Class II	Active
Implant Prosthetics	8002180	FDA UDI	Class II	Active
Fiber Technology	7009011	FDA UDI	Class II	Unknown
Astra	8006751	FDA UDI	Class I	Active
Camlog	8003530	FDA UDI	Class I	Active
Preat	710032	FDA UDI	Class II	Active
Preat	7551540	FDA UDI	Class I	Unknown
Nobel	8000541	FDA UDI	Class I	Active
Implant Prosthetics	9004432-100	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9007245	FDA UDI	Class I	Active
Preat	0809997	FDA UDI	Class II	Active
Implant Prosthetics	8001789	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006622	FDA UDI	Class II	Active
Preat	0800698	FDA UDI	Class II	Active
Preat	9000968	FDA UDI	Class II	Active
Preci-Clix	0101233-50	FDA UDI	Class I	Unknown
Sphero Attachment	0819662	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004723	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004777	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001667-F	FDA UDI	Class II	Active
Implant Prosthetics	9000281	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605701C	FDA UDI	Class II	Active
O-Ring	1701202	FDA UDI	Class II	Active
Implant Prosthetics	9001700-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000672	FDA UDI	Class II	Active
Implant Prosthetics	9000100-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9002203	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006521	FDA UDI	Class II	Active
Sphero Attachment	0822003	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601501	FDA UDI	Class II	Active
Sphero Attachment	0800040	FDA UDI	Class II	Active
Preat	1500504	FDA UDI	Class I	Active
Preat	9005355	FDA UDI	Class II	Unknown
Implant Prosthetics	9001532	FDA UDI	Class II	Unknown
Ackermann	0102108	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004781	FDA UDI	Class II	Active
O-Ring	9000020	FDA UDI	Class I	Active
Preci-Clix	1601002	FDA UDI	Class II	Active
Implant Prosthetics	9005000	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605705C	FDA UDI	Class II	Active
O-Ring	1700572	FDA UDI	Class II	Active
Implant Prosthetics	8003750	FDA UDI	Class II	Unknown
Preat	0812895	FDA UDI	Class II	Active
Sphero Attachments	0812400	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706804C	FDA UDI	Class II	Active
Sphero Flex	0828615	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606601C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005780	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005859	FDA UDI	Class II	Active
Preat	0800268	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.