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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 61 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9000803-25	FDA UDI	Class I	Unknown
Preat	3O694SI	FDA UDI	Class I	Active
Preat	9000056	FDA UDI	Class I	Active
Preat Implant Prosthetics	1600551	FDA UDI	Class II	Active
Implant Prosthetics	8000162	FDA UDI	Class II	Unknown
Implant Prosthetics	9005530	FDA UDI	Class II	Unknown
Implant Prosthetics	9004423	FDA UDI	Class II	Active
Preat	9006851	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606603C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005967	FDA UDI	Class II	Active
Preat	0819674	FDA UDI	Class II	Active
Preat	9004790	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000075	FDA UDI	Class I	Active
Implant Prosthetics	8004725	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705702C	FDA UDI	Class II	Active
Implant Prosthetics	9001832	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005762	FDA UDI	Class II	Active
Implant Prosthetics	9005835	FDA UDI	Class II	Unknown
Preat	9000055	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600602C	FDA UDI	Class II	Active
Sphero Attachments	0809683	FDA UDI	Class II	Active
Implant Prosthetics	8001081	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007154	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004703	FDA UDI	Class I	Active
Preat Implant Prosthetics	9003741	FDA UDI	Class I	Active
Preat	0809959	FDA UDI	Class II	Active
Preat	9007165-F	FDA UDI	Class II	Active
Preat	0808186	FDA UDI	Class II	Active
Preat	9002067	FDA UDI	Class II	Active
Preat	1300333	FDA UDI	Class I	Unknown
Sphero Attachment	0808452	FDA UDI	Class II	Active
Sphero	0802288	FDA UDI	Class II	Active
Implant Prosthetics	8005076	FDA UDI	Class II	Active
Preat	9005169	FDA UDI	Class II	Active
Implant Prosthetics	9001480	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006422	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004467-F	FDA UDI	Class II	Active
Nobel Active	8004730	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600304	FDA UDI	Class II	Active
Preat	0819552	FDA UDI	Class II	Active
Implant Prosthetics	9006832-10	FDA UDI	Class II	Unknown
Preat	9001795	FDA UDI	Class II	Active
Preat	3TLH13	FDA UDI	Class I	Unknown
O-Ring	1701502	FDA UDI	Class II	Active
Implant Prosthetics	9000430-10	FDA UDI	Class II	Unknown
Preat	0802073	FDA UDI	Class II	Active
Implant Prosthetics	8003485	FDA UDI	Class II	Active
Preat	1600551C	FDA UDI	Class II	Active
Preat	3O694SX	FDA UDI	Class I	Active
Implant Prosthetics	9000132-100	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.