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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 18 of 80

Device	Model / Reference	Registries	Class	Status
Sphero Attachment	0809688	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600802	FDA UDI	Class II	Active
Preat	3X693AI	FDA UDI	Class I	Active
Implant Prosthetics	8002172	FDA UDI	Class II	Active
Preat Implant Prosthetics	9008545	FDA UDI	Class I	Active
Preat	1100004	FDA UDI	Class I	Active
Preat	710654	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005701	FDA UDI	Class I	Active
Preat	9006690	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005876	FDA UDI	Class II	Active
Preat	7100020-20	FDA UDI	Class I	Active
Implant Prosthetics	8003751-10	FDA UDI	Class II	Unknown
Preat	3X0694N	FDA UDI	Class I	Active
Implant Prosthetics	8000161	FDA UDI	Class II	Unknown
Implant Prosthetics	8000185	FDA UDI	Class II	Active
Astra	8006561	FDA UDI	Class II	Active
Implant Prosthetics	8000920	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001445	FDA UDI	Class I	Active
Implant Prosthetics	9000582	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006464	FDA UDI	Class II	Active
Preat	9000261	FDA UDI	Class II	Active
Preat	9001468	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600202C	FDA UDI	Class II	Unknown
Implant Prosthetics	9000932-100	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600501	FDA UDI	Class II	Active
Preci-Clix	0101233	FDA UDI	Class I	Active
Preat	2148684	FDA UDI	Class II	Active
Preat	9000265	FDA UDI	Class II	Active
Preat	0804505-4	FDA UDI	Class I	Active
Implant Prosthetics	8004475	FDA UDI	Class II	Active
Implant Prosthetics	8000675	FDA UDI	Class II	Active
Implant Prosthetics	8001262	FDA UDI	Class II	Unknown
Preci-Sagix	0101366-6	FDA UDI	Class I	Unknown
Implant Prosthetics	8001780	FDA UDI	Class II	Active
Implant Prosthetics	9000903-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000272	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005976	FDA UDI	Class II	Active
Implant Prosthetics	9006600	FDA UDI	Class I	Active
Implant Prosthetics	9005178	FDA UDI	Class II	Active
Straumann	8001200	FDA UDI	Class I	Active
Preat	9003760-2	FDA UDI	Class II	Unknown
Preat	7550073	FDA UDI	Class I	Active
Preat	0101211	FDA UDI	Class I	Active
3i Certain	8001815	FDA UDI	Class I	Active
Preat	0813200	FDA UDI	Class II	Active
Preat	0800163	FDA UDI	Class I	Active
Implant Prosthetics	9001761	FDA UDI	Class II	Active
Inclusive	8003720	FDA UDI	Class I	Active
Preat	9003744	FDA UDI	Class II	Active
Preat	9001663	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.