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 3 of 80

Device	Model / Reference	Registries	Class	Status
Nobel	8000804	FDA UDI	Class I	Active
Preat	1600552C	FDA UDI	Class II	Unknown
Implant Prosthetics	9006832-100	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600506	FDA UDI	Class II	Active
Implant Prosthetics	8000950	FDA UDI	Class II	Active
Sphero Attachments	0811402	FDA UDI	Class II	Active
Implant Prosthetics	8004472	FDA UDI	Class II	Active
Implant Prosthetics	9001777	FDA UDI	Class II	Active
O-Ring	1500204	FDA UDI	Class I	Unknown
Preat	9006665	FDA UDI	Class II	Active
Preat	9003760	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1604701C	FDA UDI	Class II	Active
Shiner Magnet System	1422822	FDA UDI	Class II	Unknown
Preat	9000661	FDA UDI	Class II	Active
Implant Prosthetics	9000232-50	FDA UDI	Class I	Unknown
Sphero Attachments	0813073	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600576C	FDA UDI	Class II	Active
Preat	1500650	FDA UDI	Class I	Active
Preat	9005195	FDA UDI	Class II	Active
Preat	9000367	FDA UDI	Class II	Active
Preat	9003733-50	FDA UDI	Class II	Active
Preat	0809612	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006650	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004759	FDA UDI	Class II	Active
Preat	0812056	FDA UDI	Class II	Active
Astra	8006850	FDA UDI	Class II	Active
Implant Prosthetics	8000450	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001767-F	FDA UDI	Class II	Active
Implant Prosthetics	9000103-10	FDA UDI	Class I	Unknown
Zimmer	8000223	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706403C	FDA UDI	Class II	Active
Preat	7551330	FDA UDI	Class I	Unknown
Preat	2142107	FDA UDI	Class II	Active
Implant Prosthetics	8002750	FDA UDI	Class II	Unknown
Preat	9003758-10	FDA UDI	Class II	Active
Preat	9005165-F	FDA UDI	Class II	Active
Preat	9000953	FDA UDI	Class II	Active
Preat	9005069	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000038	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600404	FDA UDI	Class II	Active
Implant Prosthetics	9004700-10	FDA UDI	Class I	Unknown
Sphero Attachments	0809119	FDA UDI	Class II	Active
Preat	2239GSF	FDA UDI	Class I	Active
Sphero Attachment	0811002	FDA UDI	Class II	Active
Preat	9000995	FDA UDI	Class II	Active
Implant Prosthetics	8001462	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005961	FDA UDI	Class II	Active
Implant Prosthetics	9007150	FDA UDI	Class II	Active
Implant Prosthetics	9001000-10	FDA UDI	Class I	Unknown
Preat	2RP0096	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.