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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 66 of 80

Device	Model / Reference	Registries	Class	Status
Preat Implant Prosthetics	9005969	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605201	FDA UDI	Class I	Unknown
Preat	0819673	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601500C	FDA UDI	Class II	Active
Implant Prosthetics	9002275	FDA UDI	Class II	Active
O-Ring	1600025	FDA UDI	Class I	Active
Preat Implant Prosthetics	9001245	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601704	FDA UDI	Class II	Active
Sphero Attachments	0809115	FDA UDI	Class II	Active
Implant Prosthetics	8000325	FDA UDI	Class II	Unknown
Fiber Technology	7009070-2	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9002145	FDA UDI	Class I	Active
O-Ring	1701401	FDA UDI	Class II	Active
Implant Prosthetics	9004700-25	FDA UDI	Class I	Unknown
O-Ring	1700571	FDA UDI	Class II	Active
Sphero Attachment	0809101	FDA UDI	Class II	Active
Straumann	8001331	FDA UDI	Class II	Active
3i Certain	8001651	FDA UDI	Class I	Unknown
Sphero Attachments	0809107	FDA UDI	Class II	Active
Preat	9004964	FDA UDI	Class II	Active
Preat	9000810	FDA UDI	Class I	Active
Ankylos	8004830	FDA UDI	Class II	Active
Implant Prosthetics	9006500-25	FDA UDI	Class I	Unknown
Sphero Attachments	0819631	FDA UDI	Class II	Active
Preat	9001830	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005103	FDA UDI	Class I	Active
Preat	0822674	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004762	FDA UDI	Class II	Active
Preat	30800TI	FDA UDI	Class I	Active
Preat	0101218	FDA UDI	Class I	Unknown
Nobel	8000822	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007103	FDA UDI	Class I	Active
Preat	7551410	FDA UDI	Class I	Unknown
Preat	2142893	FDA UDI	Class II	Active
Preat	710222	FDA UDI	Class II	Active
Preat	0102010	FDA UDI	Class I	Unknown
Preat	0802797	FDA UDI	Class II	Active
Zimmer® TSV-compatible	8000240	FDA UDI	Class I	Unknown
Implant Prosthetics	9000730-10	FDA UDI	Class I	Unknown
Hader	0101746	FDA UDI	Class I	Active
Preat	2RQ031L	FDA UDI	Class I	Active
Preat	0813804	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007079	FDA UDI	Class II	Active
Preci-Clix	1600020	FDA UDI	Class I	Active
Preat	9001669	FDA UDI	Class II	Active
Preat	0809668	FDA UDI	Class II	Active
Implant Prosthetics	8003271	FDA UDI	Class II	Active
Implant Prosthetics	9001635	FDA UDI	Class II	Unknown
Preat	7551650	FDA UDI	Class I	Unknown
Splintastik	0200002	FDA UDI	Class I	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.