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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 68 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9004779	FDA UDI	Class II	Active
Preat	1500610	FDA UDI	Class I	Unknown
Preat	3X694M2	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006430	FDA UDI	Class II	Active
Equator	2149104	FDA UDI	Class II	Active
Sphero Attachment	0801503	FDA UDI	Class II	Active
Implant Prosthetics	8004972	FDA UDI	Class II	Active
Sphero Attachments	0809763	FDA UDI	Class II	Active
Implant Prosthetics	9002261	FDA UDI	Class II	Active
Astra	8006835	FDA UDI	Class II	Active
Implant Prosthetics	9003703-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9001650	FDA UDI	Class II	Active
Implant Prosthetics	8000286	FDA UDI	Class II	Active
Implant Prosthetics	8000820	FDA UDI	Class II	Active
Shiner Magnet System	1423913	FDA UDI	Class II	Unknown
Implant Prosthetics	9005635	FDA UDI	Class II	Active
Preat	0800169	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600400C	FDA UDI	Class II	Active
Implant Prosthetics	9000200	FDA UDI	Class I	Active
Preat	0809662	FDA UDI	Class II	Active
Sphero Attachments	0819614	FDA UDI	Class II	Active
Preat	2RT00A1	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005745	FDA UDI	Class I	Active
Preat	2148766	FDA UDI	Class II	Active
Implant Prosthetics	9002277	FDA UDI	Class II	Active
Preci-Clix	0101231	FDA UDI	Class I	Active
Preat	0809105	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600406C	FDA UDI	Class II	Active
Implant Prosthetics	8001661	FDA UDI	Class II	Unknown
Preat	7100021-4	FDA UDI	Class I	Active
Preci-Bar	0101114	FDA UDI	Class I	Active
Preat	0805056	FDA UDI	Class I	Active
Preat	7551530	FDA UDI	Class I	Unknown
Everstick	7009006	FDA UDI	Class I	Unknown
Preat	1600552C	FDA UDI	Class II	Active
Implant Prosthetics	8003270	FDA UDI	Class II	Active
Implant Prosthetics	9005032	FDA UDI	Class II	Unknown
Straumann	8001521	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706604C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600572C	FDA UDI	Class II	Active
Implant Prosthetics	9001675	FDA UDI	Class II	Active
Implant Prosthetics	9000154	FDA UDI	Class II	Active
Preat	1400510	FDA UDI	Class I	Unknown
Preat	0800542	FDA UDI	Class I	Active
Preci-Bar	0101113	FDA UDI	Class I	Unknown
Astra	8006530	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601403C	FDA UDI	Class II	Active
Preat	9006895	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006661	FDA UDI	Class II	Active
Preat	0102006	FDA UDI	Class I	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.