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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 48 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9001565-F	FDA UDI	Class II	Active
Equator	2149503	FDA UDI	Class II	Active
Preat	0800266	FDA UDI	Class I	Active
MicroMini	8002700	FDA UDI	Class I	Active
Preci-Bar	0101110	FDA UDI	Class I	Active
Sphero Attachments	0819613	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006635	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000703	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600102C	FDA UDI	Class II	Active
Hader	0101710	FDA UDI	Class I	Active
Nobel	8000815	FDA UDI	Class I	Active
Implant Prosthetics	9001603-25	FDA UDI	Class I	Unknown
Preat	9007095	FDA UDI	Class II	Active
Sphero Attachments	0819958	FDA UDI	Class II	Active
Preat	0101220	FDA UDI	Class I	Active
Preat	9000295	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001367-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006522	FDA UDI	Class II	Active
Implant Prosthetics	9005361	FDA UDI	Class II	Active
Sphero Attachments	0812218	FDA UDI	Class II	Active
Preat	0101297	FDA UDI	Class I	Unknown
Preat	3694C19	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004167-F	FDA UDI	Class II	Active
Preat	2140CER	FDA UDI	Class I	Active
Astra EV	8006440	FDA UDI	Class I	Unknown
Preci-Bar	0101164	FDA UDI	Class I	Active
Preat	0200040	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605301	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9000767-F	FDA UDI	Class II	Active
Preat	9000048	FDA UDI	Class I	Active
Preat	9001961	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600204	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9007078	FDA UDI	Class II	Active
Preat	9001568	FDA UDI	Class II	Active
Implant Prosthetics	8000970	FDA UDI	Class II	Active
Camlog	8003435	FDA UDI	Class II	Active
Shiner Magnet System	1429631	FDA UDI	Class II	Active
Preci-Sagix	0101357	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000967-F	FDA UDI	Class II	Active
Implant Prosthetics	8005075	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007081	FDA UDI	Class II	Active
Astra	8002204	FDA UDI	Class I	Active
Preat Implant Prosthetics	0800263	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006804	FDA UDI	Class I	Active
Fiber Technology	7009060-10	FDA UDI	Class II	Unknown
Preat	0818761	FDA UDI	Class II	Active
Preat	0819004	FDA UDI	Class II	Active
Preat	9001661	FDA UDI	Class II	Active
Implant Prosthetics	8000870	FDA UDI	Class II	Active
Preat	9001764	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.