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 13 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9005867-F	FDA UDI	Class II	Active
Implant Prosthetics	9000830	FDA UDI	Class II	Active
Imz	8005136	FDA UDI	Class II	Active
Implant Prosthetics	9007050	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007185	FDA UDI	Class II	Active
Itl	8000058	FDA UDI	Class I	Active
Nobel Active	8004930	FDA UDI	Class II	Active
Sphero Attachments	0819675	FDA UDI	Class II	Active
Preat	9000163	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005881	FDA UDI	Class II	Active
Preat	9000362	FDA UDI	Class II	Active
Preat	0804402	FDA UDI	Class II	Active
Preat	9003764	FDA UDI	Class II	Active
Itl	8000068	FDA UDI	Class I	Active
Preat	9000395	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605402	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006530	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600202C	FDA UDI	Class II	Active
Implant Prosthetics	9005150-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8001250	FDA UDI	Class II	Active
Preat	0101299	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005781	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005985	FDA UDI	Class II	Active
Gingivamoll	0906407	FDA UDI	Class I	Unknown
Implant Prosthetics	9003700	FDA UDI	Class I	Active
Preat Implant Prosthetics	8001237	FDA UDI	Class II	Active
Implant Prosthetics	9006632-50	FDA UDI	Class II	Unknown
Preat	7551820	FDA UDI	Class I	Unknown
Implant Prosthetics	8005162	FDA UDI	Class II	Active
Implant Prosthetics	9001630	FDA UDI	Class II	Unknown
Preat	9002053	FDA UDI	Class II	Active
Preat	0818758	FDA UDI	Class II	Active
O-Ring	1700575	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005403	FDA UDI	Class I	Active
Implant Prosthetics	8002176	FDA UDI	Class II	Active
Preat	7551240	FDA UDI	Class I	Unknown
Implant Prosthetics	8001461	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9005935	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705906C	FDA UDI	Class II	Active
Preat	0803302	FDA UDI	Class II	Active
Astra	8006862	FDA UDI	Class II	Active
Preat	0819722	FDA UDI	Class II	Active
Clix Attachments	1601002C	FDA UDI	Class II	Active
Preat	9001664	FDA UDI	Class II	Active
Preat	710022	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006852	FDA UDI	Class I	Active
Preat	0809673	FDA UDI	Class II	Active
Sphero Attachments	0819003	FDA UDI	Class II	Active
Preat	9006465-F	FDA UDI	Class II	Active
Preat	0801728	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.