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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 5 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	1706603C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006645	FDA UDI	Class I	Active
Preat Implant Prosthetics	1707003C	FDA UDI	Class II	Active
Preat	710053	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005467-F	FDA UDI	Class II	Active
Nobel	8000800	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000550	FDA UDI	Class II	Active
Equator	2142004	FDA UDI	Class II	Active
Preci-Sagix	0101361-6	FDA UDI	Class I	Unknown
Implant Prosthetics	8000270	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006401	FDA UDI	Class I	Active
Preat	7551550	FDA UDI	Class I	Unknown
Preat	9004765	FDA UDI	Class II	Active
Preat	3O694KN	FDA UDI	Class I	Active
Sphero Block	0804403	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004761	FDA UDI	Class II	Active
Implant Prosthetics	9000235	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1602001	FDA UDI	Class II	Unknown
Preat	0800167	FDA UDI	Class I	Active
Preat	0813301	FDA UDI	Class II	Active
Sphero Attachments	0819653	FDA UDI	Class II	Active
Implant Prosthetics	8002825	FDA UDI	Class II	Active
Implant Prosthetics	8003756	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005759	FDA UDI	Class II	Active
Preat	9002161	FDA UDI	Class II	Active
Astra	8006750	FDA UDI	Class II	Active
Preat	7551821	FDA UDI	Class I	Unknown
Preat	9004563	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005776	FDA UDI	Class II	Active
Preat	2RT0H20	FDA UDI	Class I	Active
Preat	710714	FDA UDI	Class II	Active
Nobel	8000601	FDA UDI	Class I	Active
Implant Prosthetics	8000677	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600406	FDA UDI	Class II	Active
Implant Prosthetics	9003743	FDA UDI	Class II	Unknown
Preat	9003708	FDA UDI	Class I	Active
O-Ring	1600823	FDA UDI	Class II	Active
Implant Prosthetics	9001430-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000989	FDA UDI	Class II	Active
Implant Prosthetics	8000725	FDA UDI	Class II	Unknown
Preci-Sagix	0101312-6	FDA UDI	Class I	Unknown
Straumann	8001523	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600603	FDA UDI	Class II	Active
Implant Prosthetics	8000825	FDA UDI	Class II	Active
Implant Prosthetics	8003555-10	FDA UDI	Class II	Unknown
Preat	9004469	FDA UDI	Class II	Active
Preat	0803072	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600305	FDA UDI	Class II	Active
Sphero Attachments	0819613	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1601404	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.