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 27 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9006468	FDA UDI	Class II	Active
Preat	9003795	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006403	FDA UDI	Class I	Active
Preat	0600F15	FDA UDI	Class I	Active
O-Ring	1700576	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600811C	FDA UDI	Class II	Active
O-Ring	6000005	FDA UDI	Class I	Active
Preat	9001562	FDA UDI	Class II	Active
Preat	2339SFE	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007567	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000042	FDA UDI	Class I	Active
Preat	0803401	FDA UDI	Class II	Active
Shiner Magnet System	1421202	FDA UDI	Class II	Unknown
Preat	710025	FDA UDI	Class II	Active
Preat	9005865-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006767-F	FDA UDI	Class II	Active
Equator	2148674	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001203	FDA UDI	Class I	Active
Preat	3X724C2	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605605	FDA UDI	Class II	Active
Sphero Attachment	0812004	FDA UDI	Class II	Active
Preat	9007065	FDA UDI	Class II	Active
Preat	9004751	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006724	FDA UDI	Class II	Active
Preat	9002035	FDA UDI	Class II	Active
Implant Prosthetics	9005259	FDA UDI	Class II	Active
Preat	2RPAX61	FDA UDI	Class I	Active
Implant Prosthetics	9001632-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9002150	FDA UDI	Class II	Active
Implant Prosthetics	9000900	FDA UDI	Class I	Active
Preci-Sagix	0101313-6	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600601	FDA UDI	Class II	Active
Implant Prosthetics	9000810-10	FDA UDI	Class I	Unknown
Implant Prosthetics	9002132-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8003261	FDA UDI	Class II	Active
Implant Prosthetics	9000189	FDA UDI	Class II	Active
Preat	0800240	FDA UDI	Class II	Active
Preat	0819000	FDA UDI	Class II	Active
Implant Prosthetics	9005580	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006559	FDA UDI	Class II	Active
Preat	0811005	FDA UDI	Class II	Active
Zimmer	8000109	FDA UDI	Class II	Active
Preat	1776030	FDA UDI	Class I	Active
Implant Prosthetics	8001773	FDA UDI	Class II	Active
Preat	9000495	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007001	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005875	FDA UDI	Class II	Active
Sphero Attachment	0809841	FDA UDI	Class II	Active
Preat	7551215	FDA UDI	Class I	Unknown
Preat	1700406	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.