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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 44 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9007085	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007168	FDA UDI	Class II	Active
Preci-Bar	0106905	FDA UDI	Class I	Unknown
Nobel	8000501	FDA UDI	Class I	Active
Preat	3X694AL	FDA UDI	Class I	Active
Implant Prosthetics	8001050-10	FDA UDI	Class II	Unknown
Preat	9006451	FDA UDI	Class I	Active
Preat	1500194	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601702C	FDA UDI	Class II	Active
Preat	710165	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006504	FDA UDI	Class I	Active
Mays	0200060	FDA UDI	Class I	Active
O-Ring	1701500	FDA UDI	Class II	Active
Implant Prosthetics	9000400-25	FDA UDI	Class I	Unknown
Hader Bar	0101701	FDA UDI	Class I	Unknown
Implant Prosthetics	9001681	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600803C	FDA UDI	Class II	Active
Implant Prosthetics	8000275	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006501	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605601C	FDA UDI	Class II	Active
Preat	1400305	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600302C	FDA UDI	Class II	Active
Precision Attachments	0702030	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605805C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600575	FDA UDI	Class II	Unknown
Implant Prosthetics	8000978	FDA UDI	Class II	Active
Nobel	8000915	FDA UDI	Class I	Active
Equator	2141557	FDA UDI	Class II	Active
Itl	8000054	FDA UDI	Class I	Active
Preat Implant Prosthetics	1706801C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007201	FDA UDI	Class I	Active
Preat	7551230	FDA UDI	Class I	Unknown
Implant Prosthetics	9000659	FDA UDI	Class II	Active
Zimmer	8000201	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600401C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605903C	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608005	FDA UDI	Class II	Active
Preci-Clix	0101235-6	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600204C	FDA UDI	Class II	Unknown
Implant Prosthetics	8000450-10	FDA UDI	Class II	Unknown
Preat	9004135	FDA UDI	Class II	Active
Implant Prosthetics	9005832	FDA UDI	Class II	Unknown
Sphero Attachments	0819782	FDA UDI	Class II	Active
Implant Prosthetics	9004400-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8002189	FDA UDI	Class II	Active
Implant Prosthetics	9000283	FDA UDI	Class II	Active
Preat	9004467	FDA UDI	Class II	Active
Implant Prosthetics	8002050	FDA UDI	Class II	Unknown
Preat	9003737	FDA UDI	Class II	Active
Preat	9001262	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.