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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 14 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9006490	FDA UDI	Class II	Active
Preat	9000390	FDA UDI	Class II	Active
Preat	710084	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005775	FDA UDI	Class II	Active
Preci-Vertix	0101801	FDA UDI	Class I	Active
Implant Prosthetics	9002200-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8000877	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600502	FDA UDI	Class II	Active
Preat	710043	FDA UDI	Class II	Active
Preat	9005159	FDA UDI	Class II	Active
Implant Prosthetics	9000303-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9005050	FDA UDI	Class II	Active
Sphero Attachments	0819682	FDA UDI	Class II	Active
Implant Prosthetics	9004400	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600903C	FDA UDI	Class II	Active
Preat	0101271	FDA UDI	Class I	Unknown
Preat	7551830	FDA UDI	Class I	Unknown
Preat	1400520	FDA UDI	Class I	Unknown
Preat	0818760	FDA UDI	Class II	Active
Camlog	8003635	FDA UDI	Class II	Active
Implant Prosthetics	9000178	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006659	FDA UDI	Class II	Active
Preat	9000590	FDA UDI	Class II	Active
Preat	2R185NP	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606801C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005703	FDA UDI	Class I	Active
Implant Prosthetics	9005350	FDA UDI	Class II	Active
Preat	9001465	FDA UDI	Class II	Active
Preat	3TL00H4	FDA UDI	Class I	Active
Preat	9001763	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005824	FDA UDI	Class II	Active
Sphero Attachments	0800522	FDA UDI	Class II	Active
Implant Prosthetics	8004459	FDA UDI	Class II	Unknown
Equator	2148532	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706401C	FDA UDI	Class II	Active
Fiber Technology	7009070-5	FDA UDI	Class II	Unknown
Implant Prosthetics	9005832-50	FDA UDI	Class II	Unknown
Preat	9001261	FDA UDI	Class II	Active
Preat	9004167	FDA UDI	Class II	Active
Preat	0809657	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001635	FDA UDI	Class II	Active
Preat	9005665	FDA UDI	Class II	Active
Preat	9001553	FDA UDI	Class II	Active
Implant Prosthetics	8001450	FDA UDI	Class II	Unknown
Preat	2R761TI	FDA UDI	Class I	Active
Preat	2R175NP	FDA UDI	Class I	Active
Nobel	8004710	FDA UDI	Class I	Active
Preat	9007265	FDA UDI	Class II	Active
Preat	9001263	FDA UDI	Class II	Active
Astra	8006535	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.