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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 36 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9000203-25	FDA UDI	Class I	Unknown
O-Ring	1708006	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004763	FDA UDI	Class II	Active
Implant Prosthetics	8000881	FDA UDI	Class II	Active
Preat	9005965-F	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600105	FDA UDI	Class II	Active
Sphero Attachment	0801404	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006862	FDA UDI	Class II	Active
Implant Prosthetics	9005561	FDA UDI	Class II	Active
Implant Prosthetics	9001235-10	FDA UDI	Class I	Unknown
Preci-Sagix	0101361-50	FDA UDI	Class I	Unknown
Preat	710041	FDA UDI	Class II	Active
Preat	9000964	FDA UDI	Class II	Active
Preat	2RX0150	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605606C	FDA UDI	Class II	Active
Implant Prosthetics	9006500-10	FDA UDI	Class I	Unknown
Preat	7551800	FDA UDI	Class I	Unknown
Preat	9005067	FDA UDI	Class II	Active
Preat Implant Prosthetics	1707001C	FDA UDI	Class II	Active
Implant Prosthetics	9005050-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9000532-10	FDA UDI	Class I	Unknown
Preat	1500608	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007024	FDA UDI	Class II	Active
Implant Prosthetics	9000103-25	FDA UDI	Class I	Unknown
Preat	0601251	FDA UDI	Class I	Active
Implant Prosthetics	9001500	FDA UDI	Class I	Active
Camlog	8003315	FDA UDI	Class I	Active
Preat	710651	FDA UDI	Class II	Active
Preat	9004463	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004789	FDA UDI	Class II	Active
Implant Prosthetics	9005400	FDA UDI	Class I	Active
3i Certain	8001710	FDA UDI	Class I	Active
Astra	8006650	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706501C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000235	FDA UDI	Class II	Active
Gingivamoll	0906403	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006669	FDA UDI	Class II	Active
Preat	1700906	FDA UDI	Class II	Active
Implant Prosthetics	9005400-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000850	FDA UDI	Class II	Unknown
Sphero Attachments	0818455	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706701C	FDA UDI	Class II	Active
O-Ring	1701203	FDA UDI	Class II	Active
Implant Prosthetics	9001200-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8001362	FDA UDI	Class II	Active
Implant Prosthetics	8003359	FDA UDI	Class II	Active
Nobel	8000710	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005722	FDA UDI	Class II	Active
M3	3691P00	FDA UDI	Class I	Active
Preat	0813172	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.