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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 32 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	1601004C	FDA UDI	Class II	Active
Preat	3724C29	FDA UDI	Class I	Active
Nobel	8000818	FDA UDI	Class II	Active
Astra	8002015	FDA UDI	Class I	Active
Preci-Vertix	0101800	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601604C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005535	FDA UDI	Class II	Active
Preat	9001259	FDA UDI	Class II	Active
Zimmer	8000221	FDA UDI	Class II	Active
Implant Prosthetics	9001435-10	FDA UDI	Class I	Unknown
Preat	7550025	FDA UDI	Class I	Active
Preci-Sagix	0101362-50	FDA UDI	Class I	Unknown
Preat	9001462	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605001	FDA UDI	Class II	Unknown
Implant Prosthetics	9007032-50	FDA UDI	Class II	Unknown
Preat	0822663	FDA UDI	Class II	Active
Preat	8004910	FDA UDI	Class I	Active
O-Ring	1700504	FDA UDI	Class II	Active
Implant Prosthetics	9000851	FDA UDI	Class I	Active
Shiner Magnet System	1400721	FDA UDI	Class I	Unknown
O-Ring	1705401	FDA UDI	Class II	Active
Implant Prosthetics	9000835	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004403	FDA UDI	Class I	Active
Preat	710154	FDA UDI	Class II	Active
Preat	9003763-1	FDA UDI	Class II	Active
Preat	50000-75	FDA UDI	Class II	Unknown
Preat	9001590	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006889	FDA UDI	Class II	Active
Preat	2142225	FDA UDI	Class II	Active
Preat	9001765-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	1500506	FDA UDI	Class I	Active
Equator	2148533	FDA UDI	Class II	Active
Preat Implant Prosthetics	8001741	FDA UDI	Class I	Active
Itl	8000057	FDA UDI	Class I	Active
Preat	9000047	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006564	FDA UDI	Class II	Active
Preat	0101323	FDA UDI	Class I	Active
Implant Prosthetics	8005061	FDA UDI	Class II	Active
Implant Prosthetics	8001787	FDA UDI	Class II	Active
Preci-Sagix	0101321	FDA UDI	Class I	Active
Implant Prosthetics	9004150	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705901C	FDA UDI	Class II	Active
Implant Prosthetics	8001759	FDA UDI	Class II	Unknown
Sphero Attachments	0819632	FDA UDI	Class II	Active
Sphero Attachment	0819430	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007135	FDA UDI	Class II	Active
Implant Prosthetics	9006432-10	FDA UDI	Class II	Unknown
Preat	0819683	FDA UDI	Class II	Active
Implant Prosthetics	9005630	FDA UDI	Class II	Active
Preat Implant Prosthetics	1601602	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.