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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 67 of 80

Device	Model / Reference	Registries	Class	Status
Perma Block	5851003	FDA UDI	Class I	Active
Preat	2142102	FDA UDI	Class II	Active
Preat	9006751	FDA UDI	Class I	Active
Implant Prosthetics	9000550	FDA UDI	Class II	Unknown
Preci-Sagix	0101311-50	FDA UDI	Class I	Unknown
Implant Prosthetics	9000732-50	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	8006640	FDA UDI	Class I	Unknown
Implant Prosthetics	8000150-10	FDA UDI	Class II	Unknown
Preat	710712	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605405C	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600815	FDA UDI	Class II	Active
Itl	8000055	FDA UDI	Class I	Active
Preat	0818759	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600572	FDA UDI	Class II	Unknown
Preat	7551720	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1500505	FDA UDI	Class I	Active
Preat	9002265	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005752	FDA UDI	Class I	Active
Preat	9000565	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000033	FDA UDI	Class I	Active
Implant Prosthetics	9000280	FDA UDI	Class II	Active
Nobel	8000504	FDA UDI	Class I	Active
Implant Prosthetics	9003731-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8003489	FDA UDI	Class II	Active
Preat	0819554	FDA UDI	Class II	Active
MegaGen	8004405	FDA UDI	Class I	Active
Preat	50005-25	FDA UDI	Class II	Unknown
Sphero Attachments	0801504	FDA UDI	Class II	Active
Straumann® TL-compatible	8001240	FDA UDI	Class I	Unknown
Sphero Attachments	0805201	FDA UDI	Class II	Active
Preci-Bar	0101112	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006679	FDA UDI	Class II	Active
Gingivamoll	0900001	FDA UDI	Class I	Unknown
Implant Prosthetics	8005181	FDA UDI	Class II	Active
Implant Prosthetics	9001250-10	FDA UDI	Class I	Unknown
Preat	0803808	FDA UDI	Class II	Active
Shiner Magnet System	1429764	FDA UDI	Class II	Unknown
Implant Prosthetics	9006532	FDA UDI	Class II	Unknown
Implant Prosthetics	8000180	FDA UDI	Class II	Active
Sphero Attachment	0813501	FDA UDI	Class II	Active
Shiner Magnet System	1400170	FDA UDI	Class I	Unknown
Implant Prosthetics	8001092	FDA UDI	Class II	Active
3i Certain®-compatible	9001803	FDA UDI	Class I	Active
Preat	2RT00P4	FDA UDI	Class I	Active
Preat	0818613	FDA UDI	Class II	Active
Preat	0101386	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005045	FDA UDI	Class I	Active
Preat	0101204	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005921	FDA UDI	Class II	Active
Implant Prosthetics	8004859	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.