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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 42 of 80

Device	Model / Reference	Registries	Class	Status
Preat	7551620	FDA UDI	Class I	Unknown
Preat	9004930	FDA UDI	Class II	Active
Preat	7551630	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600901	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000545	FDA UDI	Class I	Active
Preat	710662	FDA UDI	Class II	Active
Preat	9001861	FDA UDI	Class II	Active
Implant Prosthetics	9003703-10	FDA UDI	Class I	Unknown
Preat	9001667	FDA UDI	Class II	Active
Preat Implant Prosthetics	0101701	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000503	FDA UDI	Class I	Active
Preat	9005068	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601501C	FDA UDI	Class II	Active
Implant Prosthetics	9001403-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8002950	FDA UDI	Class II	Active
Preat	9005035	FDA UDI	Class II	Active
O-Ring	1500606	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606703C	FDA UDI	Class II	Active
Preat	2RT00H4	FDA UDI	Class I	Active
Sagix	0101313	FDA UDI	Class I	Active
Preat	9005163	FDA UDI	Class II	Active
Preat	9002230	FDA UDI	Class II	Active
Preat	0101291	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600405C	FDA UDI	Class II	Active
Implant Prosthetics	8004482	FDA UDI	Class I	Active
Gingivamoll	0906402	FDA UDI	Class I	Unknown
Ankylos®-compatible	8004840	FDA UDI	Class I	Unknown
3i Certain	8001810	FDA UDI	Class I	Active
Astra	8002115	FDA UDI	Class I	Active
Astra	8006668	FDA UDI	Class II	Unknown
Preat	9001690	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005867	FDA UDI	Class II	Active
Astra	8006651	FDA UDI	Class I	Active
Preat Implant Prosthetics	9002167-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000567-F	FDA UDI	Class II	Active
Preat	9000052	FDA UDI	Class I	Active
Preat	9000859	FDA UDI	Class II	Active
Sphero Attachments	0819630	FDA UDI	Class II	Active
Preat	710031	FDA UDI	Class II	Active
Implant Prosthetics	9000850	FDA UDI	Class II	Active
Sagix	0101312	FDA UDI	Class I	Active
Preat	9000169	FDA UDI	Class II	Active
Implant Prosthetics	9001232	FDA UDI	Class II	Unknown
Preat	9005265	FDA UDI	Class II	Active
Implant Prosthetics	9003750	FDA UDI	Class II	Active
Legacy	9008500	FDA UDI	Class I	Active
Preat	2141CTE	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1608001C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705803C	FDA UDI	Class II	Active
Implant Prosthetics	9001535-10	FDA UDI	Class I	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.