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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 10 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9005132-50	FDA UDI	Class II	Unknown
Preat	2RT00H5	FDA UDI	Class I	Active
Implant Prosthetics	9001622	FDA UDI	Class II	Unknown
Implant Prosthetics	8000261	FDA UDI	Class II	Unknown
Implant Prosthetics	9001551	FDA UDI	Class I	Active
Preat	9000278	FDA UDI	Class II	Active
Preat	9004963	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601405C	FDA UDI	Class II	Active
Preat	0815201	FDA UDI	Class II	Active
Preat	0809684	FDA UDI	Class II	Active
MegaGen AnyRidge®-compatible	8004440	FDA UDI	Class I	Unknown
Preat	1911802	FDA UDI	Class I	Unknown
Preat	1100003	FDA UDI	Class I	Active
Preat	3X691EO	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601502C	FDA UDI	Class II	Active
Sphero Attachments	0809635	FDA UDI	Class II	Active
Implant Prosthetics	9001432-10	FDA UDI	Class II	Unknown
Implant Prosthetics	9004900	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600201	FDA UDI	Class II	Active
Equator	2141933	FDA UDI	Class II	Active
Equator	2148116	FDA UDI	Class II	Active
Preat	2L334CX	FDA UDI	Class I	Active
Implant Prosthetics	9005280	FDA UDI	Class II	Active
Implant Prosthetics	9001481	FDA UDI	Class II	Active
Implant Prosthetics	8001475	FDA UDI	Class II	Active
Sphero Block	0809196	FDA UDI	Class II	Active
Implant Prosthetics	9000277	FDA UDI	Class II	Active
Preat	0101270	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601504	FDA UDI	Class II	Active
Preat	710153	FDA UDI	Class II	Active
O-Ring	1701504	FDA UDI	Class II	Active
Preat	9004459	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007061	FDA UDI	Class II	Active
Implant Prosthetics	9004900-10	FDA UDI	Class I	Unknown
3i Certain	8001615	FDA UDI	Class I	Active
Implant Prosthetics	9005689	FDA UDI	Class II	Active
Implant Prosthetics	8003752	FDA UDI	Class II	Unknown
Implant Prosthetics	8002181	FDA UDI	Class II	Active
Preat	710121	FDA UDI	Class II	Active
Preat	9001653	FDA UDI	Class II	Active
Implant Prosthetics	9002289	FDA UDI	Class II	Active
Preat	0803073	FDA UDI	Class II	Active
Hiossen	8005021	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600604	FDA UDI	Class II	Active
Implant Prosthetics	9004178	FDA UDI	Class II	Active
Sphero Attachment	0809842	FDA UDI	Class II	Active
O-Ring	1702201	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001630	FDA UDI	Class II	Active
Straumann	8001504	FDA UDI	Class I	Active
Implant Prosthetics	9005535	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.