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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 51 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8004925	FDA UDI	Class II	Active
Preat	1921733	FDA UDI	Class I	Unknown
Camlog	8003535	FDA UDI	Class I	Active
Preat	1300348	FDA UDI	Class I	Unknown
Implant Prosthetics	9000300-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000580	FDA UDI	Class II	Active
Fiber Technology	7009060-3	FDA UDI	Class II	Unknown
Implant Prosthetics	9000132-10	FDA UDI	Class I	Unknown
Preat	2R100TI	FDA UDI	Class I	Active
Preat	9005765	FDA UDI	Class II	Active
Preat	9000959	FDA UDI	Class II	Active
Preat	0808703	FDA UDI	Class II	Active
Preat	01K1276	FDA UDI	Class I	Active
Preat	710173	FDA UDI	Class II	Active
Preat	9000668	FDA UDI	Class II	Active
Sphero Attachments	0809960	FDA UDI	Class II	Active
Hader Bar	0101720	FDA UDI	Class I	Unknown
Preat	0817657	FDA UDI	Class II	Active
Preat	0800261	FDA UDI	Class I	Active
Implant Prosthetics	8000561	FDA UDI	Class II	Unknown
Preat	9001459	FDA UDI	Class II	Active
Implant Prosthetics	9000103	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005821	FDA UDI	Class II	Active
Implant Prosthetics	9001630-10	FDA UDI	Class II	Unknown
Preat	1400340	FDA UDI	Class I	Unknown
Implant Prosthetics	8000975	FDA UDI	Class II	Active
Implant Prosthetics	9000203-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005864	FDA UDI	Class II	Active
Sphero Attachments	0818107	FDA UDI	Class II	Active
Sphero Attachments	0809681	FDA UDI	Class II	Active
Implant Prosthetics	9003732-25	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1705902C	FDA UDI	Class II	Active
Preat	9005061	FDA UDI	Class II	Active
Implant Prosthetics	9004422	FDA UDI	Class II	Active
O-Ring	1701505	FDA UDI	Class II	Active
Preat	8004915	FDA UDI	Class I	Active
Implant Prosthetics	8002278	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006445	FDA UDI	Class I	Active
Preat	0818685	FDA UDI	Class II	Active
Preat	0800143	FDA UDI	Class I	Active
Implant Prosthetics	8000661	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600205C	FDA UDI	Class II	Active
Camlog	8003251	FDA UDI	Class I	Active
Implant Prosthetics	9000232	FDA UDI	Class I	Unknown
Zimmer	8000151	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600500C	FDA UDI	Class II	Active
Preat	0801930	FDA UDI	Class II	Active
Preat Implant Prosthetics	0108980	FDA UDI	Class II	Active
Preat	9006495	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004100	FDA UDI	Class I	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.