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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 29 of 80

Device	Model / Reference	Registries	Class	Status
Shiner Magnet System	1400641	FDA UDI	Class I	Unknown
Sphero Attachments	0800142	FDA UDI	Class I	Active
Preat	1600036	FDA UDI	Class I	Active
Sphero Attachment	0819664	FDA UDI	Class II	Active
Implant Prosthetics	8001450-10	FDA UDI	Class II	Active
Preat	0802801	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007203	FDA UDI	Class I	Active
Implant Prosthetics	9005032-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9001735-10	FDA UDI	Class II	Unknown
Preat	710221	FDA UDI	Class II	Active
Preat	9005661	FDA UDI	Class II	Active
Implant Prosthetics	9003763-2	FDA UDI	Class II	Unknown
Preat	9005167	FDA UDI	Class II	Active
Implant Prosthetics	9003735	FDA UDI	Class II	Unknown
Nobel	8000819	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005345	FDA UDI	Class I	Active
Implant Prosthetics	9001250	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605001C	FDA UDI	Class I	Unknown
Implant Prosthetics	9003763	FDA UDI	Class II	Unknown
Preat	1400335	FDA UDI	Class I	Unknown
Nobel	8000441	FDA UDI	Class I	Active
Shiner Magnet System	1400001	FDA UDI	Class I	Unknown
Fiber Technology	7009060-2	FDA UDI	Class II	Unknown
Implant Prosthetics	9000950	FDA UDI	Class II	Active
Preat	9000965	FDA UDI	Class II	Active
Sphero Block	0802628	FDA UDI	Class II	Active
Preat	9000567	FDA UDI	Class II	Active
Preat	9001767	FDA UDI	Class II	Active
Preat	9006890	FDA UDI	Class II	Active
Preat	50000-25	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9007267	FDA UDI	Class II	Active
Preat	0800147	FDA UDI	Class I	Active
Ackermann	0102118	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006404	FDA UDI	Class I	Active
Preat	710144	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004767-F	FDA UDI	Class II	Active
Preat	2140CEG	FDA UDI	Class I	Active
Preat	1500605	FDA UDI	Class I	Active
Preat	1500508	FDA UDI	Class I	Unknown
Implant Prosthetics	8001859	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605401C	FDA UDI	Class II	Active
Perma Ret	0109004	FDA UDI	Class I	Active
Preat	9000667	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000603	FDA UDI	Class I	Active
Preat	9005795	FDA UDI	Class II	Active
Preat	9005062	FDA UDI	Class II	Active
Implant Prosthetics	9001603	FDA UDI	Class I	Active
Sphero Attachment	0801730	FDA UDI	Class II	Active
Sphero Attachments	0811405	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600303	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.