Is this your brand? Sign in to claim ownership.

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 63 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9005051	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600903	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600203C	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600205	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600401	FDA UDI	Class II	Active
Sphero Attachments	0800140	FDA UDI	Class I	Active
Implant Prosthetics	8001020	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9001645	FDA UDI	Class I	Active
Preat	9000462	FDA UDI	Class II	Active
O-Ring	1702203	FDA UDI	Class II	Active
Preat	9000565-F	FDA UDI	Class II	Active
Preat	9005367	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007223	FDA UDI	Class II	Active
Implant Prosthetics	8000476	FDA UDI	Class II	Active
Preat Implant Prosthetics	1707101C	FDA UDI	Class II	Active
Implant Prosthetics	9000632	FDA UDI	Class I	Unknown
Preat	9005865	FDA UDI	Class II	Active
Preat	9000259	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600505	FDA UDI	Class II	Active
O-Ring	1708004	FDA UDI	Class II	Active
Preat	9004464	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001845	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006861	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005980	FDA UDI	Class II	Active
Implant Prosthetics	9003751-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9005132	FDA UDI	Class II	Unknown
Implant Prosthetics	8000470	FDA UDI	Class II	Active
Preat	1500615	FDA UDI	Class I	Active
Implant Prosthetics	9006700	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600504	FDA UDI	Class II	Active
Sphero Attachment	0819655	FDA UDI	Class II	Active
Preat	1500506-2	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1600821C	FDA UDI	Class II	Unknown
Implant Prosthetics	9000181	FDA UDI	Class II	Active
O-Ring	1705404	FDA UDI	Class II	Active
Preat	1921732	FDA UDI	Class I	Unknown
Sphero Attachments	0814011	FDA UDI	Class II	Active
Implant Prosthetics	9003736-100	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1601403	FDA UDI	Class II	Active
Sphero Attachments	0809167	FDA UDI	Class II	Active
Preat	0101230	FDA UDI	Class I	Unknown
Implant Prosthetics	9001775	FDA UDI	Class II	Active
Preat	0600F11	FDA UDI	Class I	Unknown
Camlog	8003551	FDA UDI	Class I	Active
Preat	0801929	FDA UDI	Class II	Active
Zimmer	8000202	FDA UDI	Class I	Active
Preat	9007090	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005789	FDA UDI	Class II	Active
Preat	1500200	FDA UDI	Class I	Active
Preat	0101281	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.