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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 78 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9007062	FDA UDI	Class II	Active
Preat Implant Prosthetics	9003723	FDA UDI	Class II	Active
Implant Prosthetics	8003481	FDA UDI	Class II	Active
Implant Prosthetics	8001776	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007130	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006561	FDA UDI	Class II	Active
Implant Prosthetics	8001677	FDA UDI	Class II	Active
O-Ring	1701703	FDA UDI	Class II	Active
Implant Prosthetics	9004932-50	FDA UDI	Class II	Unknown
O-Ring	1700605	FDA UDI	Class II	Active
Implant Prosthetics	9001450	FDA UDI	Class II	Active
Sphero Attachment	0822733	FDA UDI	Class II	Active
Implant Prosthetics	8003471	FDA UDI	Class II	Active
Implant Prosthetics	9001580	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600901C	FDA UDI	Class II	Active
Zimmer	8000205	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006752	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004767	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000335	FDA UDI	Class II	Active
MegaGen	8004419	FDA UDI	Class II	Active
Implant Prosthetics	9005180	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006768	FDA UDI	Class II	Active
Astra	8002135	FDA UDI	Class II	Active
Implant Prosthetics	8003562	FDA UDI	Class II	Active
Preat Implant Prosthetics	8000735	FDA UDI	Class II	Active
Sphero	0802289	FDA UDI	Class II	Active
Hader Bar	0101704-50	FDA UDI	Class I	Unknown
Implant Prosthetics	8003377	FDA UDI	Class II	Active
O-Ring Implant Abutments	1500246	FDA UDI	Class II	Unknown
Implant Prosthetics	9001732-50	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1705801C	FDA UDI	Class II	Active
Implant Prosthetics	9002276	FDA UDI	Class II	Active
Camlog	8003335	FDA UDI	Class II	Active
Implant Prosthetics	8001962	FDA UDI	Class II	Active
Implant Prosthetics	8001681	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705704C	FDA UDI	Class II	Active
Preci-Clix	0101235	FDA UDI	Class I	Unknown
Sphero Attachments	0809922	FDA UDI	Class II	Active
Implant Prosthetics	8000420	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601506C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005845	FDA UDI	Class I	Active
Preat Implant Prosthetics	1706803C	FDA UDI	Class II	Active
O-Ring	1702103	FDA UDI	Class II	Active
Implant Prosthetics	8004870	FDA UDI	Class II	Active
Implant Prosthetics	9006532-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8002170	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600556	FDA UDI	Class II	Unknown
Equator	2148629	FDA UDI	Class II	Active
Implant Prosthetics	9004481	FDA UDI	Class II	Active
Implant Prosthetics	9000935-10	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.