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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 19 of 80

Device	Model / Reference	Registries	Class	Status
Branemark	8001035	FDA UDI	Class II	Active
Equator	2142002	FDA UDI	Class II	Active
Implant Prosthetics	9004432-10	FDA UDI	Class II	Unknown
Preat	0819995	FDA UDI	Class II	Active
Preat	9000365-F	FDA UDI	Class II	Active
Implant Prosthetics	9004403-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1605406C	FDA UDI	Class II	Active
Astra	8006669	FDA UDI	Class II	Unknown
Preat	9000465	FDA UDI	Class II	Active
Implant Prosthetics	9001203-10	FDA UDI	Class I	Unknown
Preat	9000464	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005877	FDA UDI	Class II	Active
Preat	9001662	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006735	FDA UDI	Class II	Active
Preat Implant Prosthetics	9008567-F	FDA UDI	Class II	Active
Preat	20760CE	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000245	FDA UDI	Class I	Active
Preat	9000269	FDA UDI	Class II	Active
Implant Prosthetics	9001789	FDA UDI	Class II	Active
Sphero Attachments	0809645	FDA UDI	Class II	Active
Implant Prosthetics	9006732-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8000875	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600500	FDA UDI	Class II	Active
Preat	0101303	FDA UDI	Class I	Unknown
Implant Prosthetics	8000271	FDA UDI	Class II	Active
Preat	710223	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600402	FDA UDI	Class II	Active
Preci-Vertix	0101845	FDA UDI	Class I	Active
Preat	9005065-F	FDA UDI	Class II	Active
Preat	7550055	FDA UDI	Class I	Active
Sagix	0101366	FDA UDI	Class I	Active
Implant Prosthetics	9000432	FDA UDI	Class I	Unknown
Sphero Attachment	0802004	FDA UDI	Class II	Active
Preat	710054	FDA UDI	Class II	Active
Preat	9001461	FDA UDI	Class II	Active
Implant Prosthetics	9000150	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001735	FDA UDI	Class II	Active
Implant Prosthetics	9006700-10	FDA UDI	Class I	Unknown
Sphero Block	0802425	FDA UDI	Class II	Active
Keystone	8005840	FDA UDI	Class I	Unknown
Preat	0802002	FDA UDI	Class II	Active
Implant Prosthetics	8000850-10	FDA UDI	Class II	Unknown
Preat	9004465-F	FDA UDI	Class II	Active
Preat	9006551	FDA UDI	Class I	Active
Preat	0800710	FDA UDI	Class II	Active
Hader Bar	0112340	FDA UDI	Class I	Active
Preat	0802894	FDA UDI	Class II	Active
Implant Prosthetics	9000732-100	FDA UDI	Class I	Unknown
Astra	8006430	FDA UDI	Class II	Active
Implant Prosthetics	9004935-10	FDA UDI	Class II	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.