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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 20 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8001150	FDA UDI	Class II	Active
Preat	0103004	FDA UDI	Class I	Active
Implant Prosthetics	9007032	FDA UDI	Class II	Unknown
Equator	2146902	FDA UDI	Class II	Active
Preat	0822310	FDA UDI	Class II	Active
Preat	710172	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006550	FDA UDI	Class II	Active
Implant Prosthetics	9005562	FDA UDI	Class II	Unknown
Implant Prosthetics	8001486	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007235	FDA UDI	Class II	Active
Hader Bar	0101709-50	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005823	FDA UDI	Class II	Active
Preat	9004495	FDA UDI	Class II	Active
Preat Implant Prosthetics	1607004C	FDA UDI	Class II	Active
Implant Prosthetics	9000932-10	FDA UDI	Class I	Unknown
Preat	7551605	FDA UDI	Class I	Unknown
Preat	3X694AR	FDA UDI	Class I	Active
Sphero Flex	0822069	FDA UDI	Class II	Active
Implant Prosthetics	8004871	FDA UDI	Class II	Active
Implant Prosthetics	8001581	FDA UDI	Class II	Active
Preat	0800155	FDA UDI	Class I	Active
Hader Bar	0101709	FDA UDI	Class I	Unknown
Legacy	9005603	FDA UDI	Class I	Active
Preat Implant Prosthetics	9004780	FDA UDI	Class II	Active
Preat	9003768	FDA UDI	Class II	Active
Implant Prosthetics	9005489	FDA UDI	Class II	Active
Implant Prosthetics	8000659	FDA UDI	Class II	Active
Sphero Attachment	0823813	FDA UDI	Class II	Active
Preat	0102005	FDA UDI	Class I	Active
Preat	9005359	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005763	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606501C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001867-F	FDA UDI	Class II	Active
Implant Prosthetics	9002232-50	FDA UDI	Class II	Unknown
Implant Prosthetics	8000480	FDA UDI	Class II	Active
Preat	710094	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006567-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006667	FDA UDI	Class II	Active
Astra	8006559	FDA UDI	Class II	Active
Implant Prosthetics	9003756-10	FDA UDI	Class II	Unknown
Preat	9000264	FDA UDI	Class II	Active
Sphero Attachments	0809631	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000065	FDA UDI	Class I	Active
Implant Prosthetics	9000950	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9007230	FDA UDI	Class II	Active
Implant Prosthetics	9001530-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000425	FDA UDI	Class II	Active
Zimmer	8000215	FDA UDI	Class I	Active
Implant Prosthetics	9004903-10	FDA UDI	Class I	Active
Preat	0819551	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.