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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 33 of 80

Device	Model / Reference	Registries	Class	Status
Preat	9000465-F	FDA UDI	Class II	Active
CAMLOG® Screw-Line-compatible	8003541	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005667-F	FDA UDI	Class II	Active
Preat	2330SBE	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006868	FDA UDI	Class II	Active
Preat	9004753	FDA UDI	Class II	Active
Nobel	8004701	FDA UDI	Class I	Active
3i Certain	8001941	FDA UDI	Class I	Active
Sphero Attachments	0819771	FDA UDI	Class II	Active
Implant Prosthetics	8005177	FDA UDI	Class II	Active
Preci-Clix	0101232W-6	FDA UDI	Class I	Unknown
O-Ring	1500630-4	FDA UDI	Class I	Unknown
Preat	9001867	FDA UDI	Class II	Active
Implant Prosthetics	9001601	FDA UDI	Class I	Active
Implant Prosthetics	9004450	FDA UDI	Class II	Active
Shiner Magnet System	1429686	FDA UDI	Class II	Unknown
Preat	1911732	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006845	FDA UDI	Class I	Active
Implant Prosthetics	8003387	FDA UDI	Class II	Active
Implant Prosthetics	8003662	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600104C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9004445	FDA UDI	Class I	Active
Preat	9000895	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600501C	FDA UDI	Class II	Active
Preat	3O694SN	FDA UDI	Class I	Active
Preat	9004130	FDA UDI	Class II	Active
Nobel	8000801	FDA UDI	Class I	Active
Preat	0813080	FDA UDI	Class II	Active
Preat	1500634	FDA UDI	Class I	Active
Preat	2RT00P7	FDA UDI	Class I	Active
Preat	9000053	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006461	FDA UDI	Class II	Active
Preat	3X694A2	FDA UDI	Class I	Active
Camlog	8003515	FDA UDI	Class I	Active
Preat Implant Prosthetics	1704704C	FDA UDI	Class II	Active
Preat	7551510	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1706504C	FDA UDI	Class II	Active
Preat	7551210	FDA UDI	Class I	Unknown
Preat	0802799	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000110	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600904	FDA UDI	Class II	Active
Implant Prosthetics	8004962	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605704C	FDA UDI	Class II	Active
Astra	8006562	FDA UDI	Class II	Active
Wagner	7008002	FDA UDI	Class I	Active
Preat	0101276	FDA UDI	Class I	Active
Preat	0809780	FDA UDI	Class II	Active
Preat Implant Prosthetics	1604401	FDA UDI	Class II	Unknown
Hiossen	8005023	FDA UDI	Class II	Active
Implant Prosthetics	9002132-50	FDA UDI	Class II	Unknown

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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.