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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 49 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9000435-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9004432-50	FDA UDI	Class II	Unknown
Implant Prosthetics	9001703-10	FDA UDI	Class II	Unknown
Preat	01K1251	FDA UDI	Class I	Active
Preat	9005235	FDA UDI	Class II	Active
Implant Prosthetics	8003561	FDA UDI	Class II	Active
Camlog	8003341	FDA UDI	Class I	Active
Preat	3694C20	FDA UDI	Class I	Active
Implant Prosthetics	9000632-50	FDA UDI	Class I	Unknown
Nobel	8000510	FDA UDI	Class I	Active
Preat Implant Prosthetics	9002067-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606503C	FDA UDI	Class II	Active
Implant Prosthetics	9004700	FDA UDI	Class I	Active
Implant Prosthetics	9001403-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9003731-50	FDA UDI	Class II	Unknown
Implant Prosthetics	8003259	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005959	FDA UDI	Class II	Active
Zimmer	8000121	FDA UDI	Class II	Active
O-Ring	1776005	FDA UDI	Class I	Active
Preat Implant Prosthetics	9008567	FDA UDI	Class II	Active
Implant Prosthetics	8004861	FDA UDI	Class II	Active
Fiber Technology	7009008	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1608004	FDA UDI	Class II	Active
Implant Prosthetics	8000320	FDA UDI	Class II	Unknown
Preat	9007295	FDA UDI	Class II	Active
Preat	0800611	FDA UDI	Class I	Active
Preat	9005135	FDA UDI	Class II	Active
Implant Prosthetics	9000203	FDA UDI	Class I	Active
A. Titan	8000005	FDA UDI	Class I	Active
Implant Prosthetics	8002261	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006667-F	FDA UDI	Class II	Active
Implant Prosthetics	9006600-10	FDA UDI	Class I	Unknown
Universal IC Attachment	1200112	FDA UDI	Class I	Active
Sphero Attachment	0802003	FDA UDI	Class II	Active
Implant Prosthetics	8000973	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605906C	FDA UDI	Class II	Active
Implant Prosthetics	9000800-10	FDA UDI	Class I	Unknown
3i Certain	8001830	FDA UDI	Class II	Active
Astra	8002130	FDA UDI	Class II	Active
Preat	9000469	FDA UDI	Class II	Active
Implant Prosthetics	8004471	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600104	FDA UDI	Class II	Active
Implant Prosthetics	8000575	FDA UDI	Class II	Active
Implant Prosthetics	9004477	FDA UDI	Class II	Active
Sphero Attachments	0800757	FDA UDI	Class II	Active
Sphero Attachment	0801403	FDA UDI	Class II	Active
Implant Prosthetics	9001432	FDA UDI	Class II	Unknown
Implant Prosthetics	8005072	FDA UDI	Class II	Active
Sphero Attachments	0809630	FDA UDI	Class II	Active
Implant Prosthetics	9001900-25	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.