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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 60 of 80

Device	Model / Reference	Registries	Class	Status
Perma Ret	0109002	FDA UDI	Class I	Active
Preat	9007195	FDA UDI	Class II	Active
Preat	1600037	FDA UDI	Class I	Active
Implant Prosthetics	8003479	FDA UDI	Class II	Active
Implant Prosthetics	8005171	FDA UDI	Class II	Active
Preat	0809434	FDA UDI	Class II	Active
Implant Prosthetics	8003487	FDA UDI	Class II	Active
Implant Prosthetics	8002177	FDA UDI	Class II	Active
Sphero Attachments	0819650	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9003703	FDA UDI	Class I	Active
Implant Prosthetics	9005103-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9000877	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705805C	FDA UDI	Class II	Active
Preat	9001490	FDA UDI	Class II	Active
Implant Prosthetics	8001959	FDA UDI	Class II	Active
Implant Prosthetics	9001632	FDA UDI	Class II	Unknown
Implant Prosthetics	9000303-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9005089	FDA UDI	Class II	Active
Preat	0101350	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007104	FDA UDI	Class I	Active
Preat Implant Driver Tools	9000031	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600103	FDA UDI	Class II	Active
Implant Prosthetics	9001051	FDA UDI	Class I	Active
Nobel	8004901	FDA UDI	Class I	Active
O-Ring	1500601	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006624	FDA UDI	Class II	Active
Hiossen	8005118	FDA UDI	Class II	Active
Sphero Attachments	0813069	FDA UDI	Class II	Active
Shiner Magnet System	1400701	FDA UDI	Class I	Unknown
Implant Prosthetics	8002725	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000135	FDA UDI	Class II	Active
Hader	0101731	FDA UDI	Class I	Active
Preat	2R161NP	FDA UDI	Class I	Active
Preat	1500507	FDA UDI	Class I	Active
Preat	9001569	FDA UDI	Class II	Active
Sphero Attachments	0800651	FDA UDI	Class II	Active
Implant Prosthetics	8001676	FDA UDI	Class II	Active
Implant Prosthetics	9000889	FDA UDI	Class II	Active
Preat	710212	FDA UDI	Class II	Active
Preat Implant Prosthetics	8001231	FDA UDI	Class II	Unknown
Preci-Clix	0101232W	FDA UDI	Class I	Active
Hiossen	8005104	FDA UDI	Class I	Active
Preat	710016	FDA UDI	Class II	Active
Preat	9005265-F	FDA UDI	Class II	Active
Preat	9005765-F	FDA UDI	Class II	Active
Preat	7551340	FDA UDI	Class I	Unknown
Preat	9002267	FDA UDI	Class II	Active
Hader	0101120	FDA UDI	Class I	Active
Preat	7551400	FDA UDI	Class I	Unknown
Preat	9000365	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.