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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 53 of 80

Device	Model / Reference	Registries	Class	Status
Sphero Block	0808612	FDA UDI	Class II	Active
Preat	9004453	FDA UDI	Class II	Active
eFiber	7009055	FDA UDI	Class II	Unknown
Preat	0102003	FDA UDI	Class I	Unknown
Preat	9000867	FDA UDI	Class II	Active
Preat	0102008	FDA UDI	Class I	Active
Hader	0101765	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005861	FDA UDI	Class II	Active
Preat	710716	FDA UDI	Class II	Active
Preat	710674	FDA UDI	Class II	Active
Preat	9006765	FDA UDI	Class II	Active
Sphero Attachment	0800830	FDA UDI	Class II	Active
Implant Prosthetics	8005081	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001745	FDA UDI	Class I	Active
Preat Implant Prosthetics	1600555C	FDA UDI	Class II	Active
Nobel	8004751	FDA UDI	Class I	Active
Implant Prosthetics	8000862	FDA UDI	Class II	Unknown
Sphero Attachments	0819701	FDA UDI	Class II	Active
Preat	0809994	FDA UDI	Class II	Active
Sphero Attachments	0809432	FDA UDI	Class II	Active
Sphero Attachment	0823913	FDA UDI	Class II	Active
Sphero Attachments	0800653	FDA UDI	Class II	Unknown
Preci-Bar	0101106	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9004769	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006552	FDA UDI	Class I	Active
Preat	9001453	FDA UDI	Class II	Active
Straumann	8001423	FDA UDI	Class II	Active
Preat	2140CEV	FDA UDI	Class I	Active
Implant Prosthetics	9000980	FDA UDI	Class II	Active
Preat	9000630	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005767	FDA UDI	Class II	Active
Preat	1400320	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1606701C	FDA UDI	Class II	Active
Preat	7551815	FDA UDI	Class I	Unknown
Implant Prosthetics	9004435-10	FDA UDI	Class II	Unknown
Sphero Attachments	0809430	FDA UDI	Class II	Active
Implant Prosthetics	9002061	FDA UDI	Class II	Active
Preat	30885TI	FDA UDI	Class I	Active
Preci-Sagix	0101366-50	FDA UDI	Class I	Unknown
Implant Prosthetics	9000900-10	FDA UDI	Class I	Unknown
Sphero Attachment	0809655	FDA UDI	Class II	Active
O-Ring	1701603	FDA UDI	Class II	Active
Implant Prosthetics	8002259	FDA UDI	Class II	Active
Equator	2142073	FDA UDI	Class II	Active
Implant Prosthetics	8000520	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600823C	FDA UDI	Class II	Unknown
Branemark	8004177	FDA UDI	Class II	Active
Fiber Technology	7009030	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005267-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9002267-F	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.