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 12 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8000175	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007163	FDA UDI	Class II	Active
Preat	0809647	FDA UDI	Class II	Active
Implant Prosthetics	9000900-25	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006764	FDA UDI	Class II	Active
Preat Implant Driver Tools	9000044	FDA UDI	Class I	Active
Preat Implant Prosthetics	1604703C	FDA UDI	Class II	Active
Equator	2148531	FDA UDI	Class II	Active
Sphero Block	0808702	FDA UDI	Class II	Active
Straumann	8001515	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006454	FDA UDI	Class II	Active
Preat	9006765-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006469	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600505C	FDA UDI	Class II	Active
Preat	0800157	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606802C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006563	FDA UDI	Class II	Active
Implant Prosthetics	9005500	FDA UDI	Class I	Active
Preat	0812057	FDA UDI	Class II	Active
Implant Prosthetics	9001550	FDA UDI	Class II	Active
Preat	9001768	FDA UDI	Class II	Active
Implant Prosthetics	8001775	FDA UDI	Class II	Active
Preat	0808699	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006767	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005962	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606403C	FDA UDI	Class II	Active
Preat	0809106	FDA UDI	Class II	Active
Astra	8006550	FDA UDI	Class II	Active
Implant Prosthetics	9000551	FDA UDI	Class I	Active
Preat	710013	FDA UDI	Class II	Active
Implant Prosthetics	9000500	FDA UDI	Class I	Active
Implant Prosthetics	9001875	FDA UDI	Class II	Active
Preat	9002165-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007181	FDA UDI	Class II	Active
Implant Prosthetics	9006732	FDA UDI	Class II	Unknown
Preat Implant Driver Tools	9000039	FDA UDI	Class I	Active
Implant Prosthetics	8000662	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005203	FDA UDI	Class I	Active
Preat	0818612	FDA UDI	Class II	Active
Implant Prosthetics	8001876	FDA UDI	Class II	Active
Sphero Attachments	0819665	FDA UDI	Class II	Active
O-Ring	1701404	FDA UDI	Class II	Active
Implant Prosthetics	8003370	FDA UDI	Class II	Active
Implant Prosthetics	9000876	FDA UDI	Class II	Active
Implant Prosthetics	9002000	FDA UDI	Class I	Active
Sphero Attachments	0829118	FDA UDI	Class II	Active
Implant Prosthetics	9001900-10	FDA UDI	Class I	Unknown
Preat	8003758	FDA UDI	Class I	Active
Preat	2149558	FDA UDI	Class II	Active
Preat	710033	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.