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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 73 of 80

Device	Model / Reference	Registries	Class	Status
O-Ring	1600822	FDA UDI	Class II	Active
Implant Prosthetics	8001325	FDA UDI	Class II	Active
Implant Prosthetics	8001875	FDA UDI	Class II	Active
O-Ring	1708001	FDA UDI	Class II	Active
O-Ring	1700501	FDA UDI	Class II	Active
Implant Prosthetics	8002281	FDA UDI	Class II	Active
Preat	9003767	FDA UDI	Class II	Unknown
Preat	0822664	FDA UDI	Class II	Active
Preat	1100001	FDA UDI	Class I	Active
O-Ring	1708003	FDA UDI	Class II	Active
Implant Prosthetics	8000461	FDA UDI	Class II	Active
Hader	0101742	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000467-F	FDA UDI	Class II	Active
Preat	7551710	FDA UDI	Class I	Unknown
Implant Prosthetics	8003472	FDA UDI	Class II	Active
Preat	9000369	FDA UDI	Class II	Active
O-Ring	1500602-6	FDA UDI	Class I	Unknown
Preat	710175	FDA UDI	Class II	Active
Implant Prosthetics	9003751	FDA UDI	Class II	Active
Preat	0808652	FDA UDI	Class II	Active
Preat	9001265	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004754	FDA UDI	Class II	Active
Zimmer	8000103	FDA UDI	Class I	Active
Implant Prosthetics	9005276	FDA UDI	Class II	Active
Preat	1500503	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606804C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006475	FDA UDI	Class II	Active
Sagix	0101362	FDA UDI	Class I	Active
A. Titan	8000007	FDA UDI	Class I	Active
Implant Prosthetics	9001780	FDA UDI	Class II	Active
Astra	8006662	FDA UDI	Class II	Active
Implant Prosthetics	8000281	FDA UDI	Class II	Active
Implant Prosthetics	8000925	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004145	FDA UDI	Class I	Active
Shiner Magnet System	1400004	FDA UDI	Class I	Unknown
Preat Implant Driver Tools	9000071	FDA UDI	Class I	Active
Sphero Attachments	0800652	FDA UDI	Class II	Active
Preci-Bar	0101115	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007189	FDA UDI	Class II	Active
Implant Prosthetics	9004900-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8001087	FDA UDI	Class II	Active
Implant Prosthetics	8001091	FDA UDI	Class II	Active
Implant Prosthetics	9004903-25	FDA UDI	Class I	Unknown
MegaGen	8004404	FDA UDI	Class I	Active
Fiber Technology	7009011-12	FDA UDI	Class II	Unknown
Implant Prosthetics	9005410-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9000267-F	FDA UDI	Class II	Active
Astra	8002010	FDA UDI	Class I	Active
Preci-Clix	0101232W-50	FDA UDI	Class I	Unknown
Nobel	8000615	FDA UDI	Class I	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.