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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 40 of 80

Device	Model / Reference	Registries	Class	Status
Preat	7551310	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006523	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006554	FDA UDI	Class II	Active
MegaGen AnyRidge®-compatible	8004451	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004745	FDA UDI	Class I	Active
Preat	1300300	FDA UDI	Class I	Unknown
Preat	9005365	FDA UDI	Class II	Active
Preat	9000561	FDA UDI	Class II	Active
Preat	2RQ0033	FDA UDI	Class I	Active
Implant Prosthetics	9005003-10	FDA UDI	Class I	Unknown
Preat	1500610	FDA UDI	Class I	Active
Preat	0800151	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005410	FDA UDI	Class I	Active
Preat	9000969	FDA UDI	Class II	Active
Implant Prosthetics	9003756	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000036	FDA UDI	Class I	Active
Preat	9000265-F	FDA UDI	Class II	Active
Preat	0109003	FDA UDI	Class I	Active
Preat	2142791	FDA UDI	Class II	Active
Implant Prosthetics	9003702	FDA UDI	Class I	Active
Preat Implant Prosthetics	1601604	FDA UDI	Class II	Active
Implant Prosthetics	9004425	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1602204C	FDA UDI	Class II	Active
Preci-Sagix	0101313-50	FDA UDI	Class I	Unknown
Implant Prosthetics	8004476	FDA UDI	Class II	Active
Sphero Attachment	0819628	FDA UDI	Class II	Active
Implant Prosthetics	9005376	FDA UDI	Class II	Active
Preat	0101223	FDA UDI	Class I	Active
Implant Prosthetics	9001581	FDA UDI	Class II	Active
Preat	1776010	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007101	FDA UDI	Class I	Active
Preat Implant Prosthetics	9001267-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706402C	FDA UDI	Class II	Active
Implant Prosthetics	9005462	FDA UDI	Class II	Unknown
Preat	0800267	FDA UDI	Class I	Active
Preat	710353	FDA UDI	Class II	Active
Preat	9003733	FDA UDI	Class II	Active
Preat	9001559	FDA UDI	Class II	Active
Preat	0811400	FDA UDI	Class II	Active
Clix Attachments	1602202C	FDA UDI	Class II	Active
Implant Prosthetics	9000600-25	FDA UDI	Class I	Unknown
Preat	30295IR	FDA UDI	Class I	Active
Preat	2142903	FDA UDI	Class II	Active
Implant Prosthetics	9006832-50	FDA UDI	Class II	Unknown
Zimmer	8000141	FDA UDI	Class I	Active
Implant Prosthetics	9001000	FDA UDI	Class I	Active
Preat	0809834	FDA UDI	Class II	Active
Implant Prosthetics	8004786	FDA UDI	Class II	Active
Preat	9005053	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605601	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.