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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 71 of 80

Device	Model / Reference	Registries	Class	Status
Preat	2RT0P25	FDA UDI	Class I	Active
Preat	0804504-4	FDA UDI	Class I	Active
Implant Prosthetics	9005932-100	FDA UDI	Class II	Unknown
Preat	2RQ0032	FDA UDI	Class I	Active
Implant Prosthetics	9004478	FDA UDI	Class II	Active
Sphero Block	0802529	FDA UDI	Class II	Active
Implant Prosthetics	9000575	FDA UDI	Class II	Active
Preat	0818108	FDA UDI	Class II	Active
Implant Prosthetics	8004770	FDA UDI	Class II	Active
Implant Prosthetics	9007580	FDA UDI	Class II	Unknown
O-Ring	1600825	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601405	FDA UDI	Class II	Active
Preat	0101217	FDA UDI	Class I	Active
Preat	9004968	FDA UDI	Class II	Active
Sphero Attachment	0809103	FDA UDI	Class II	Active
Shiner Magnet System	1400711	FDA UDI	Class I	Unknown
Shiner Magnet System	1400000	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9007069	FDA UDI	Class II	Active
Astra	8006759	FDA UDI	Class II	Active
NobelActive™/Conical-compatible	8004940	FDA UDI	Class I	Unknown
Implant Prosthetics	9003705	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605703C	FDA UDI	Class II	Active
Preat	7551415	FDA UDI	Class I	Unknown
Sphero Attachments	0819001	FDA UDI	Class II	Active
Implant Prosthetics	9001676	FDA UDI	Class II	Active
Sphero Attachments	0809068	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005880	FDA UDI	Class II	Active
Sphero Attachments	0822950	FDA UDI	Class II	Active
Preat	30275TI	FDA UDI	Class I	Active
Astra	8002210	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006664	FDA UDI	Class II	Active
Preci-Sagix	0101363-6	FDA UDI	Class I	Unknown
Preat	0101227B	FDA UDI	Class I	Unknown
Implant Prosthetics	8004470	FDA UDI	Class II	Active
Implant Prosthetics	8001961	FDA UDI	Class II	Active
Implant Prosthetics	8005178	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600405	FDA UDI	Class II	Active
Implant Prosthetics	9005081	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001467-F	FDA UDI	Class II	Active
Preat	50000-16P	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1605706C	FDA UDI	Class II	Active
Preat	710664	FDA UDI	Class II	Active
Implant Prosthetics	8002185	FDA UDI	Class II	Active
Preat	9000562	FDA UDI	Class II	Active
Preat	9000563	FDA UDI	Class II	Active
Preat	9001295	FDA UDI	Class II	Active
Preat	2RQ0093	FDA UDI	Class I	Active
Preci-Sagix	0101358	FDA UDI	Class I	Active
Preat	0101213	FDA UDI	Class I	Active
Keystone	8005740	FDA UDI	Class I	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.