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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 23 of 80

Device	Model / Reference	Registries	Class	Status
Preat	0808432	FDA UDI	Class II	Active
Preat	30265TI	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007167-F	FDA UDI	Class II	Active
Preat	9001230	FDA UDI	Class II	Active
Preat	9001561	FDA UDI	Class II	Active
Implant Prosthetics	9005054	FDA UDI	Class II	Active
Preat	2RT0H12	FDA UDI	Class I	Active
Preat	2335CSB	FDA UDI	Class I	Active
Preat	2R175TI	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006568	FDA UDI	Class II	Active
Preat	9005667	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004721	FDA UDI	Class II	Active
Preat	0819199	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705802C	FDA UDI	Class II	Active
Implant Prosthetics	8000471	FDA UDI	Class II	Active
Sphero Attachment	0811404	FDA UDI	Class II	Active
Implant Prosthetics	9003741	FDA UDI	Class II	Unknown
Preat	2R785TI	FDA UDI	Class I	Active
Preat	9001769	FDA UDI	Class II	Active
Shiner Magnet System	1400012	FDA UDI	Class I	Unknown
3i Certain®-compatible	9001903	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606803C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006524	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600573	FDA UDI	Class II	Unknown
Preat	7551250	FDA UDI	Class I	Unknown
Implant Prosthetics	9001432-100	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005863	FDA UDI	Class II	Active
Astra	8002123	FDA UDI	Class II	Active
Preat	2149501	FDA UDI	Class II	Active
Preat	9004462	FDA UDI	Class II	Active
Preat	1708002	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605604C	FDA UDI	Class II	Active
Implant Prosthetics	9001732-100	FDA UDI	Class II	Unknown
Clix Attachments	1602104	FDA UDI	Class II	Active
Wagner	7008001	FDA UDI	Class I	Active
Astra	8006762	FDA UDI	Class II	Unknown
Preat	9000045	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005764	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705904C	FDA UDI	Class II	Active
Preat	0800194	FDA UDI	Class I	Active
Equator	2141250	FDA UDI	Class II	Active
Implant Prosthetics	9000200-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006569	FDA UDI	Class II	Active
Sphero Attachments	0801001	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007021	FDA UDI	Class II	Active
Implant Prosthetics	9001400	FDA UDI	Class I	Active
Preat	7551910	FDA UDI	Class I	Unknown
CAMLOG® Screw-Line-compatible	8003441	FDA UDI	Class I	Active
Preat	2148768	FDA UDI	Class II	Active
Implant Prosthetics	9003736-25	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.