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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 2 of 80

Device	Model / Reference	Registries	Class	Status
O-Ring	1700901	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600801C	FDA UDI	Class II	Active
Sphero Attachments	0819002	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600301	FDA UDI	Class II	Active
Branemark	8004175	FDA UDI	Class II	Unknown
Gingivamoll	0906405	FDA UDI	Class I	Unknown
Gingivamoll	0900003	FDA UDI	Class I	Unknown
Preat	7550051	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	8000730	FDA UDI	Class II	Active
Implant Prosthetics	8001650-10	FDA UDI	Class II	Active
Implant Prosthetics	8000481	FDA UDI	Class II	Active
O-Ring	1500630	FDA UDI	Class I	Active
Implant Prosthetics	8001559	FDA UDI	Class II	Active
Implant Prosthetics	9003730-25	FDA UDI	Class II	Unknown
Implant Prosthetics	8005071	FDA UDI	Class II	Active
Implant Prosthetics	8001473	FDA UDI	Class II	Active
O-Ring	1700604	FDA UDI	Class II	Active
Preat	0112300	FDA UDI	Class I	Active
Preat	01K1261	FDA UDI	Class I	Active
Preat	2335SBC	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005963	FDA UDI	Class II	Active
Implant Prosthetics	9006800-10	FDA UDI	Class I	Unknown
Preat	8003702	FDA UDI	Class I	Unknown
Equator	2144433	FDA UDI	Class II	Active
Preat Implant Prosthetics	1704703C	FDA UDI	Class II	Active
Preat	0819104	FDA UDI	Class II	Active
Preat	30275NP	FDA UDI	Class I	Active
Preat	9005753	FDA UDI	Class II	Active
Preat	7551840	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006654	FDA UDI	Class II	Active
O-Ring	1701503	FDA UDI	Class II	Active
Preat	9001967	FDA UDI	Class II	Active
Preat	9000162	FDA UDI	Class II	Active
Implant Prosthetics	9003757	FDA UDI	Class II	Active
Implant Prosthetics	8001261	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600813	FDA UDI	Class II	Active
Preat Implant Prosthetics	1602202	FDA UDI	Class II	Active
Implant Prosthetics	9005732-100	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1601500	FDA UDI	Class II	Active
O-Ring	1700500	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600400	FDA UDI	Class II	Active
Implant Prosthetics	9001786	FDA UDI	Class II	Unknown
Implant Prosthetics	9000600	FDA UDI	Class I	Active
Sphero Attachments	0813067	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606604C	FDA UDI	Class II	Active
Preat	9000459	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005567-F	FDA UDI	Class II	Active
Preat	9000165-F	FDA UDI	Class II	Active
Implant Prosthetics	8004759	FDA UDI	Class II	Active
Preat	0828756	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.