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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 47 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9005161	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006545	FDA UDI	Class I	Active
Preat	710672	FDA UDI	Class II	Active
Implant Prosthetics	9004932-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005923	FDA UDI	Class II	Active
Preat	1500157	FDA UDI	Class I	Unknown
Preci 52	0101566	FDA UDI	Class I	Active
Straumann	8001100	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600404C	FDA UDI	Class II	Active
Branemark	8002900	FDA UDI	Class I	Unknown
Implant Prosthetics	8001762	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1605606	FDA UDI	Class II	Active
Preat	0800200	FDA UDI	Class I	Active
Preat	3O694RN	FDA UDI	Class I	Active
Sphero Attachment	0819764	FDA UDI	Class II	Active
Implant Prosthetics	9005154	FDA UDI	Class II	Active
Preat	2142080	FDA UDI	Class II	Active
Preat	2148742	FDA UDI	Class II	Active
Implant Prosthetics	8004461	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9003735	FDA UDI	Class II	Active
Preat	9000463	FDA UDI	Class II	Active
Preat	710092	FDA UDI	Class II	Active
Preat	9004468	FDA UDI	Class II	Active
Neoss	8004165	FDA UDI	Class II	Unknown
Preat	7551900	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	8000090	FDA UDI	Class I	Unknown
Preat	6035102	FDA UDI	Class I	Active
Implant Prosthetics	8005089	FDA UDI	Class II	Active
Camlog	8003540	FDA UDI	Class I	Unknown
Implant Prosthetics	8000477	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600105C	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608002C	FDA UDI	Class II	Active
Preat	0819676	FDA UDI	Class II	Active
Implant Prosthetics	9000110	FDA UDI	Class I	Unknown
Nobel	8004904	FDA UDI	Class I	Active
Sphero Attachments	0800146	FDA UDI	Class I	Active
Implant Prosthetics	9002280	FDA UDI	Class II	Active
Preat	7100018-10	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006604	FDA UDI	Class I	Active
Implant Prosthetics	9004930-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1606504C	FDA UDI	Class II	Active
Nobel	8000604	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600902C	FDA UDI	Class II	Active
Implant Prosthetics	9003730	FDA UDI	Class II	Unknown
Implant Prosthetics	9001600	FDA UDI	Class I	Active
Implant Prosthetics	8002071	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006854	FDA UDI	Class II	Active
Preat	0604066	FDA UDI	Class I	Active
Preat	9006651	FDA UDI	Class I	Active
Preat	0819801	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.