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 77 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9007052	FDA UDI	Class I	Active
Nobel	8000410	FDA UDI	Class I	Active
Implant Prosthetics	9000532-50	FDA UDI	Class I	Unknown
O-Ring	1700401	FDA UDI	Class II	Active
Implant Prosthetics	8001873	FDA UDI	Class II	Active
Implant Prosthetics	8000821	FDA UDI	Class II	Active
Implant Prosthetics	8003250	FDA UDI	Class II	Active
Implant Prosthetics	8000159	FDA UDI	Class II	Unknown
Inclusive	8003706	FDA UDI	Class II	Active
Perma Block	5851000	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007123	FDA UDI	Class II	Active
Implant Prosthetics	9004424	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601004	FDA UDI	Class II	Active
Preat Implant Prosthetics	1604401C	FDA UDI	Class II	Unknown
Implant Prosthetics	9006400-25	FDA UDI	Class II	Unknown
Sphero Attachments	0819997	FDA UDI	Class II	Active
Sphero Block	0809702	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006576	FDA UDI	Class II	Active
Implant Prosthetics	9004451	FDA UDI	Class I	Active
Nobel	8000904	FDA UDI	Class I	Active
Implant Prosthetics	8000573	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601602C	FDA UDI	Class II	Active
O-Ring	1701200	FDA UDI	Class II	Active
Implant Prosthetics	9003707	FDA UDI	Class I	Active
Sphero Attachments	0800697	FDA UDI	Class II	Active
Implant Prosthetics	9000932	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005754	FDA UDI	Class II	Active
Implant Prosthetics	9003732-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8001478	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600806	FDA UDI	Class II	Active
Implant Prosthetics	8005172	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005067-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006435	FDA UDI	Class II	Active
Implant Prosthetics	9004732-100	FDA UDI	Class II	Unknown
Implant Prosthetics	8000586	FDA UDI	Class II	Active
Implant Prosthetics	8001872	FDA UDI	Class II	Active
Neoss	8004160	FDA UDI	Class II	Unknown
Implant Prosthetics	8001561	FDA UDI	Class II	Unknown
Implant Prosthetics	9000175	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005730	FDA UDI	Class II	Active
Sphero Attachments	803202	FDA UDI	Class II	Active
Implant Prosthetics	8001877	FDA UDI	Class II	Active
Implant Prosthetics	8000170	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600573C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005885	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005303	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000745	FDA UDI	Class I	Active
Hader Bar	0101745	FDA UDI	Class I	Active
Implant Prosthetics	8002280	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600304C	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.