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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 15 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8000921	FDA UDI	Class II	Active
Implant Prosthetics	9000503-25	FDA UDI	Class I	Unknown
Preat	2148174	FDA UDI	Class II	Active
O-Ring	9000000	FDA UDI	Class I	Active
Preat	0813806	FDA UDI	Class II	Active
Preci-Bar	010110	FDA UDI	Class I	Active
Clix Ball Implant Abutments	0108980	FDA UDI	Class II	Unknown
Sphero Attachment	0802400	FDA UDI	Class II	Active
Preat	1300342	FDA UDI	Class I	Unknown
Implant Prosthetics	8001861	FDA UDI	Class II	Active
Itl	8000035	FDA UDI	Class I	Unknown
Implant Prosthetics	8002286	FDA UDI	Class II	Active
Shiner Magnet System	1400013	FDA UDI	Class I	Unknown
Sphero Attachment	0823077	FDA UDI	Class II	Active
Implant Prosthetics	8001772	FDA UDI	Class II	Active
Sphero Attachment	0800653	FDA UDI	Class II	Active
Implant Prosthetics	8002171	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605404	FDA UDI	Class II	Active
Implant Prosthetics	9005932	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9006462	FDA UDI	Class II	Active
Preat	0808656	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006463	FDA UDI	Class II	Active
Astra®-compatible	8002050	FDA UDI	Class II	Active
Preat	710161	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007167	FDA UDI	Class II	Active
Preat	0102007	FDA UDI	Class I	Active
Preat	0809687	FDA UDI	Class II	Active
O-Ring	1705604	FDA UDI	Class II	Active
Preat Implant Prosthetics	9002103	FDA UDI	Class I	Active
O-Ring	1700603	FDA UDI	Class II	Active
Preat	2RQ0064	FDA UDI	Class I	Active
Preci-Sagix	0101307	FDA UDI	Class I	Active
Implant Prosthetics	9006532-50	FDA UDI	Class II	Unknown
Sphero Block	0803201	FDA UDI	Class II	Active
Implant Prosthetics	9005450	FDA UDI	Class II	Active
Preat	0818109	FDA UDI	Class II	Active
Implant Prosthetics	9005500-10	FDA UDI	Class I	Unknown
Equator	2142797	FDA UDI	Class II	Active
Implant Prosthetics	8000550	FDA UDI	Class II	Active
Implant Prosthetics	8000361	FDA UDI	Class II	Active
Zimmer	8000315	FDA UDI	Class I	Active
Stick®	7009071	FDA UDI	Class I	Active
3i Certain	8001930	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600822C	FDA UDI	Class II	Unknown
Straumann	8001551	FDA UDI	Class I	Unknown
Implant Prosthetics	9001832-100	FDA UDI	Class II	Unknown
Shiner Magnet System	1400140	FDA UDI	Class I	Unknown
Implant Prosthetics	9000400	FDA UDI	Class I	Active
Gingivamoll	0906410	FDA UDI	Class I	Unknown
Preat	9000690	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.