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 41 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	1605804C	FDA UDI	Class II	Active
Preat	0808924	FDA UDI	Class II	Active
Implant Prosthetics	8000587	FDA UDI	Class II	Active
Sphero Attachments	0813813	FDA UDI	Class II	Active
Implant Prosthetics	9000832-100	FDA UDI	Class I	Unknown
Preat	0101221	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006567	FDA UDI	Class II	Active
Sphero Attachment	0803914	FDA UDI	Class II	Active
Fiber Technology	7009040	FDA UDI	Class II	Unknown
Implant Prosthetics	8002276	FDA UDI	Class II	Active
Preat	7009012	FDA UDI	Class II	Unknown
Sphero Attachments	0829677	FDA UDI	Class II	Active
Preat	0800154	FDA UDI	Class I	Active
Preat	0801933	FDA UDI	Class II	Active
Itl	8000052	FDA UDI	Class I	Active
Nobil	0102000	FDA UDI	Class I	Unknown
Implant Prosthetics	8001361	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600816	FDA UDI	Class II	Active
Sphero Attachment	0801004	FDA UDI	Class II	Active
Sphero Attachments	0813075	FDA UDI	Class II	Active
Camlog	8003430	FDA UDI	Class II	Active
Preat	7551450	FDA UDI	Class I	Unknown
Preat	9000863	FDA UDI	Class II	Active
Implant Prosthetics	8004450-10	FDA UDI	Class I	Active
Hader	0101760	FDA UDI	Class I	Active
Implant Prosthetics	8001085	FDA UDI	Class II	Active
Preat	0101316	FDA UDI	Class I	Active
Preat	9001495	FDA UDI	Class II	Active
Preat	710141	FDA UDI	Class II	Active
Preat	9002271	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601401	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600571C	FDA UDI	Class II	Active
Implant Prosthetics	9005403	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006589	FDA UDI	Class II	Active
Hader	0101741	FDA UDI	Class I	Active
Preat Implant Prosthetics	1606404C	FDA UDI	Class II	Active
Implant Prosthetics	9000981	FDA UDI	Class II	Active
Preat	9006665-F	FDA UDI	Class II	Active
Preat	9004161	FDA UDI	Class II	Active
O-Ring	1700400	FDA UDI	Class II	Active
Ankylos	8004806	FDA UDI	Class I	Active
Implant Prosthetics	8001777	FDA UDI	Class II	Active
Preat	9000961	FDA UDI	Class II	Active
Hiossen	8005123	FDA UDI	Class II	Active
Itl	8000028	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1608003C	FDA UDI	Class II	Active
Implant Prosthetics	8000985	FDA UDI	Class II	Active
Preat	0819625	FDA UDI	Class II	Active
O-Ring	1705603	FDA UDI	Class II	Active
Preat	0101229	FDA UDI	Class I	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.