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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 22 of 80

Device	Model / Reference	Registries	Class	Status
Preci-Sagix	0101308	FDA UDI	Class I	Active
Implant Prosthetics	8001082	FDA UDI	Class II	Active
Preat	50005-16	FDA UDI	Class II	Unknown
Implant Prosthetics	9004903	FDA UDI	Class I	Active
Preat	710653	FDA UDI	Class II	Active
Implant Prosthetics	9001900	FDA UDI	Class I	Active
Preat	9001865	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006824	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006662	FDA UDI	Class II	Active
Implant Prosthetics	9005735	FDA UDI	Class II	Unknown
Preat	3694KS2	FDA UDI	Class I	Active
Preat	0819763	FDA UDI	Class II	Active
Implant Prosthetics	9001700-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000577	FDA UDI	Class II	Active
Implant Prosthetics	9000335	FDA UDI	Class I	Unknown
Preat	0800699	FDA UDI	Class II	Active
Implant Prosthetics	8001881	FDA UDI	Class II	Active
Nobel	8000791	FDA UDI	Class I	Unknown
Implant Prosthetics	8001761	FDA UDI	Class II	Active
Preat	9006595	FDA UDI	Class II	Active
Preat	0101216	FDA UDI	Class I	Unknown
Implant Prosthetics	8001084	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600605C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000430	FDA UDI	Class II	Active
Implant Prosthetics	9005189	FDA UDI	Class II	Active
Branemark	8001051	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005803	FDA UDI	Class I	Active
Preat	9007053	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001345	FDA UDI	Class I	Active
NobelBiocare™ Tri-Lobe-compatible	8000630	FDA UDI	Class II	Active
Preat	9001469	FDA UDI	Class II	Active
Preat	0803799	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006750	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000130	FDA UDI	Class II	Active
Preat	2148763	FDA UDI	Class II	Active
Implant Prosthetics	8004480	FDA UDI	Class I	Active
Preat	710715	FDA UDI	Class II	Active
Preat	710142	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000132	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005967-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	1707004C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005750	FDA UDI	Class II	Active
Nobel	8000591	FDA UDI	Class I	Unknown
Equator	239SFE2	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007067	FDA UDI	Class II	Active
Implant Prosthetics	9005250	FDA UDI	Class II	Active
Implant Prosthetics	9004420	FDA UDI	Class II	Active
Preat	0814406	FDA UDI	Class II	Active
Preat	710174	FDA UDI	Class II	Active
Implant Prosthetics	9007032-10	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.