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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 55 of 80

Device	Model / Reference	Registries	Class	Status
Preat	2142105	FDA UDI	Class II	Active
Sphero Block	0814501	FDA UDI	Class II	Active
Preat	0800264	FDA UDI	Class I	Active
Sphero Attachment	0803913	FDA UDI	Class II	Active
Implant Prosthetics	8002250	FDA UDI	Class II	Active
Implant Prosthetics	9001876	FDA UDI	Class II	Active
Implant Prosthetics	9000832-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9000454	FDA UDI	Class II	Active
Implant Prosthetics	8000273	FDA UDI	Class II	Active
Preat	9004465	FDA UDI	Class II	Active
Implant Prosthetics	8000259	FDA UDI	Class II	Unknown
Implant Prosthetics	9001800-25	FDA UDI	Class I	Unknown
O-Ring	1500502	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005245	FDA UDI	Class I	Active
Preat	9007265-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007263	FDA UDI	Class II	Active
Preat	9002065-F	FDA UDI	Class II	Active
Implant Prosthetics	9004428	FDA UDI	Class II	Active
Astra	8002230	FDA UDI	Class II	Active
Equator	2148120	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005769	FDA UDI	Class II	Active
Preat	0817654	FDA UDI	Class II	Active
Preat	0101331	FDA UDI	Class I	Active
O-Ring	1700902	FDA UDI	Class II	Active
MegaGen	8004423	FDA UDI	Class II	Active
Implant Prosthetics	9000603-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9005932-50	FDA UDI	Class II	Unknown
3i Certain	8001715	FDA UDI	Class I	Active
Preat	0200020	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005300	FDA UDI	Class I	Active
Implant Prosthetics	9004430-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1605604	FDA UDI	Class II	Active
Solnit	6035105	FDA UDI	Class I	Active
Implant Prosthetics	8004477	FDA UDI	Class II	Active
Implant Prosthetics	8005073	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600804	FDA UDI	Class II	Active
Preci-Vertix	0101803	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000367-F	FDA UDI	Class II	Active
Preat	9001567	FDA UDI	Class II	Active
Preat	2141CAE	FDA UDI	Class I	Active
Sphero Attachments	0801729	FDA UDI	Class II	Active
Sphero Attachments	0800655	FDA UDI	Class II	Active
Gingivamoll	0900004	FDA UDI	Class I	Unknown
Sphero Block	0818658	FDA UDI	Class II	Active
Implant Prosthetics	9004482	FDA UDI	Class II	Active
Implant Prosthetics	8001320	FDA UDI	Class II	Active
Implant Prosthetics	8002273	FDA UDI	Class II	Active
Implant Prosthetics	8001786	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005503	FDA UDI	Class I	Active
Preat Implant Prosthetics	1600554	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.