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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 58 of 80

Device	Model / Reference	Registries	Class	Status
Preat	0600F16	FDA UDI	Class I	Active
Preat	0809824	FDA UDI	Class II	Active
Implant Prosthetics	8004771	FDA UDI	Class II	Active
Preat	710023	FDA UDI	Class II	Active
Preat	9000361	FDA UDI	Class II	Active
Implant Prosthetics	8001236	FDA UDI	Class II	Unknown
Sphero Attachment	0819431	FDA UDI	Class II	Active
Implant Prosthetics	9000450	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004764	FDA UDI	Class II	Active
Preat	9000553	FDA UDI	Class II	Active
Implant Prosthetics	9006432-50	FDA UDI	Class II	Unknown
Preat	1705601	FDA UDI	Class II	Active
Implant Prosthetics	9000330-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000959	FDA UDI	Class II	Unknown
O-Ring	1701501	FDA UDI	Class II	Active
Sphero Attachments	0809926	FDA UDI	Class II	Active
Straumann	8001510	FDA UDI	Class I	Active
Implant Prosthetics	8002061	FDA UDI	Class II	Active
Ceka	3ZCS330	FDA UDI	Class II	Active
Gingivamoll	0906406	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600905C	FDA UDI	Class II	Active
Camlog	8003600	FDA UDI	Class I	Active
Preat	7100019-10	FDA UDI	Class I	Active
Preat	0818553	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600203	FDA UDI	Class II	Unknown
3i Certain	8001610	FDA UDI	Class I	Active
Implant Prosthetics	9000975	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005367-F	FDA UDI	Class II	Active
Preat	7551740	FDA UDI	Class I	Unknown
Implant Prosthetics	9000932-50	FDA UDI	Class I	Unknown
Preat	0819684	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600201C	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600802C	FDA UDI	Class II	Active
Preat	1400525	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600100C	FDA UDI	Class II	Active
Preat	0818630	FDA UDI	Class II	Active
Preat	2RP0095	FDA UDI	Class I	Active
Preat	0804501-4	FDA UDI	Class I	Active
Preat	0109005	FDA UDI	Class I	Active
Implant Prosthetics	9005289	FDA UDI	Class II	Active
Implant Prosthetics	9000832	FDA UDI	Class II	Unknown
Preat	0800650	FDA UDI	Class II	Active
Implant Prosthetics	8000181	FDA UDI	Class II	Active
Preat	0101251	FDA UDI	Class I	Unknown
Implant Prosthetics	8001472	FDA UDI	Class II	Active
Implant Prosthetics	8001580	FDA UDI	Class II	Active
Implant Prosthetics	8004961	FDA UDI	Class II	Unknown
Fiber Technology	7009060	FDA UDI	Class II	Active
Implant Prosthetics	9000150-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9002200-25	FDA UDI	Class I	Unknown

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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.