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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 11 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8002250-10	FDA UDI	Class II	Unknown
Preat	9005530	FDA UDI	Class II	Active
Implant Prosthetics	8000171	FDA UDI	Class II	Active
Shiner Magnet System	1429664	FDA UDI	Class II	Unknown
O-Ring	1500205	FDA UDI	Class I	Active
Implant Prosthetics	8002159	FDA UDI	Class II	Active
Preat	0101374	FDA UDI	Class I	Active
Zimmer	8000105	FDA UDI	Class I	Active
Hader	0101709	FDA UDI	Class I	Active
Preat	710123	FDA UDI	Class II	Active
Preat	3X694S2	FDA UDI	Class I	Active
Preat	710711	FDA UDI	Class II	Active
Preat	9000167	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004776	FDA UDI	Class II	Active
Preat	9005065	FDA UDI	Class II	Active
Preat	1400315	FDA UDI	Class I	Unknown
Implant Prosthetics	8001459	FDA UDI	Class II	Unknown
Implant Prosthetics	8000525	FDA UDI	Class II	Unknown
Implant Prosthetics	8000459	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005724	FDA UDI	Class II	Active
Preat	1911833	FDA UDI	Class I	Unknown
Implant Prosthetics	9001632-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9001200-10	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600605	FDA UDI	Class II	Active
Inclusive	8003725	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006867-F	FDA UDI	Class II	Active
Sphero Attachments	0809118	FDA UDI	Class II	Active
Preat	30261NP	FDA UDI	Class I	Active
Equator	2148451	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600575C	FDA UDI	Class II	Active
Preat	9001367	FDA UDI	Class II	Active
Preat	9006753	FDA UDI	Class II	Active
Preat	710051	FDA UDI	Class II	Active
Implant Prosthetics	9004732-50	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9002045	FDA UDI	Class I	Active
Preat	0101236D-6	FDA UDI	Class I	Unknown
Preat	9002059	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000030	FDA UDI	Class I	Active
Preat	3O694KS	FDA UDI	Class I	Active
Implant Prosthetics	9005400-10	FDA UDI	Class I	Unknown
Nobel	8000823	FDA UDI	Class II	Active
Implant Prosthetics	9003730	FDA UDI	Class II	Active
Preat	0822225	FDA UDI	Class II	Active
Implant Prosthetics	8001050	FDA UDI	Class II	Active
Implant Prosthetics	9000600-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000773	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007089	FDA UDI	Class II	Active
Sphero Block	0808935	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004768	FDA UDI	Class II	Active
Astra	8006659	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.