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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 79 of 80

Device	Model / Reference	Registries	Class	Status
Astra	8006830	FDA UDI	Class II	Active
Preci-Vertix	0101843	FDA UDI	Class I	Active
Equator	2148760	FDA UDI	Class II	Active
Implant Prosthetics	8004959	FDA UDI	Class II	Active
O-Ring	1701406	FDA UDI	Class II	Active
Implant Prosthetics	9000850-10	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007000	FDA UDI	Class I	Active
Implant Prosthetics	9000135	FDA UDI	Class I	Unknown
Equator	2142895	FDA UDI	Class II	Active
Equator	2142894	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001545	FDA UDI	Class I	Active
O-Ring	1600824	FDA UDI	Class II	Active
Sphero Attachment	0813076	FDA UDI	Class II	Active
Preat Implant Prosthetics	1604704C	FDA UDI	Class II	Active
Implant Prosthetics	9006732-100	FDA UDI	Class II	Unknown
Keystone	8005940	FDA UDI	Class I	Unknown
Astra	8002104	FDA UDI	Class I	Active
Preat Implant Driver Tools	9000032	FDA UDI	Class I	Active
Nobel	8000415	FDA UDI	Class I	Active
Implant Prosthetics	9000576	FDA UDI	Class II	Active
Sagix	0101361	FDA UDI	Class I	Active
Equator	2148535	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007164	FDA UDI	Class II	Active
Preat Implant Prosthetics	8000033	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006864	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600204	FDA UDI	Class II	Active
Implant Prosthetics	8000489	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706702C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006877	FDA UDI	Class II	Active
Sphero Attachments	0802000	FDA UDI	Class II	Active
Nobel	8000401	FDA UDI	Class I	Active
Implant Prosthetics	9007132-10	FDA UDI	Class II	Unknown
Preci-Sagix	0101314	FDA UDI	Class I	Active
Implant Prosthetics	8003756-10	FDA UDI	Class II	Unknown
Neoss	8004166	FDA UDI	Class II	Unknown
Implant Prosthetics	8000889	FDA UDI	Class II	Active
Sphero Attachments	0829656	FDA UDI	Class II	Active
O-Ring Implant Abutments	1500345	FDA UDI	Class II	Unknown
Implant Prosthetics	9002232	FDA UDI	Class II	Unknown
Sphero Block	0808994	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000034	FDA UDI	Class I	Active
Sphero Attachment	0809686	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600100	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600815C	FDA UDI	Class II	Active
Implant Prosthetics	8003371	FDA UDI	Class II	Active
Implant Prosthetics	9000880	FDA UDI	Class II	Active
O-Ring	1500630-2	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1600821C	FDA UDI	Class II	Active
Preat Abutments	K220823	FDA 510(k)	Class II	Active
Preat Abutments	K183518	FDA 510(k)	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.