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 74 of 80

Device	Model / Reference	Registries	Class	Status
Legacy-compatible	9007503	FDA UDI	Class I	Active
Implant Prosthetics	9005151	FDA UDI	Class I	Active
Sphero Attachments	0811003	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9006859	FDA UDI	Class II	Active
Implant Prosthetics	9000978	FDA UDI	Class II	Active
Hiossen® HG-compatible	8005151	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605402C	FDA UDI	Class II	Active
NobelActive™/Conical-compatible	8004740	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1500241	FDA UDI	Class II	Unknown
Shiner Magnet System	1429763	FDA UDI	Class II	Unknown
Nobel	8000740	FDA UDI	Class I	Unknown
Nobel	8000951	FDA UDI	Class I	Active
Implant Prosthetics	9005032-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9002232-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9005480	FDA UDI	Class II	Active
Clix Ball Implant Abutments	0108909	FDA UDI	Class II	Active
Implant Prosthetics	9003750-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8001659	FDA UDI	Class II	Unknown
Implant Prosthetics	8000761	FDA UDI	Class II	Active
Sphero Attachment	0819757	FDA UDI	Class II	Active
Implant Prosthetics	8000278	FDA UDI	Class II	Active
Astra	8006735	FDA UDI	Class II	Active
Astra® EV-compatible	8006740	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1607001C	FDA UDI	Class II	Active
Implant Prosthetics	8001781	FDA UDI	Class II	Active
Nobel	8004700	FDA UDI	Class I	Unknown
Implant Prosthetics	9000430	FDA UDI	Class II	Unknown
Implant Prosthetics	8000277	FDA UDI	Class II	Active
Sphero Attachment	0819685	FDA UDI	Class II	Active
MegaGen	8004418	FDA UDI	Class II	Active
Implant Prosthetics	9005461	FDA UDI	Class II	Active
Straumann® TL WN-compatible	9001303	FDA UDI	Class I	Active
Implant Prosthetics	8002920	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006575	FDA UDI	Class II	Active
Implant Prosthetics	9006832	FDA UDI	Class II	Unknown
Implant Prosthetics	9001532-50	FDA UDI	Class II	Unknown
Equator	2142333	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007076	FDA UDI	Class II	Active
Branemark	8001041	FDA UDI	Class I	Active
Preci-Sagix	0101325	FDA UDI	Class I	Active
Implant Prosthetics	9003732-2	FDA UDI	Class II	Unknown
Astra	8002223	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005868	FDA UDI	Class II	Active
Astra® EV-compatible	8006840	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005721	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005723	FDA UDI	Class II	Active
Implant Prosthetics	8000262	FDA UDI	Class II	Unknown
Neoss	8004161	FDA UDI	Class II	Unknown
Implant Prosthetics	9000800	FDA UDI	Class I	Active
Implant Prosthetics	9005435	FDA UDI	Class II	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.