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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 37 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8002062	FDA UDI	Class II	Active
Sphero Attachment	0819761	FDA UDI	Class II	Active
Implant Prosthetics	8003575	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005735	FDA UDI	Class II	Active
Preat	9001253	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706502C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006777	FDA UDI	Class II	Active
Sphero Attachments	0800500	FDA UDI	Class II	Active
Preat	2RT0H13	FDA UDI	Class I	Active
Preat	710024	FDA UDI	Class II	Active
O-Ring	1700403	FDA UDI	Class II	Active
Implant Prosthetics	9001730-10	FDA UDI	Class II	Unknown
O-Ring	1500506	FDA UDI	Class I	Unknown
Preci-Clix	0101231-6	FDA UDI	Class I	Unknown
Preat	9000368	FDA UDI	Class II	Active
Preat	9001564	FDA UDI	Class II	Active
Preat	75555555	FDA UDI	Class I	Active
Preat	9000665	FDA UDI	Class II	Active
Preci-Sagix	0101371	FDA UDI	Class I	Active
Preat	0101207	FDA UDI	Class I	Active
Preat Implant Prosthetics	1707104C	FDA UDI	Class II	Active
Implant Prosthetics	9000577	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600206	FDA UDI	Class II	Active
Implant Prosthetics	9005680	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004778	FDA UDI	Class II	Active
Implant Prosthetics	9000451	FDA UDI	Class I	Active
Preat	239SFE2	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9000167-F	FDA UDI	Class II	Active
Preat	9000669	FDA UDI	Class II	Active
Preat	9000765	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605401	FDA UDI	Class II	Unknown
Implant Prosthetics	8000449	FDA UDI	Class II	Active
Implant Prosthetics	8000673	FDA UDI	Class II	Active
Shiner Magnet System	1429685	FDA UDI	Class II	Unknown
Preat	9003733-100	FDA UDI	Class II	Active
O-Ring	1705606	FDA UDI	Class II	Active
Implant Prosthetics	8000625	FDA UDI	Class II	Unknown
Implant Prosthetics	8000986	FDA UDI	Class II	Active
Preat	1300352	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9002245	FDA UDI	Class I	Active
Implant Prosthetics	9005500-25	FDA UDI	Class I	Unknown
Preat	9007190	FDA UDI	Class II	Active
Implant Prosthetics	9003762	FDA UDI	Class II	Unknown
Implant Prosthetics	9006500	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1602104C	FDA UDI	Class II	Active
Sagix	0101363	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006623	FDA UDI	Class II	Active
NobelActive™/Conical-compatible	8000840	FDA UDI	Class I	Unknown
Preat	0101298	FDA UDI	Class I	Active
Sphero Attachment	0819728	FDA UDI	Class II	Active

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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.