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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 76 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9005132-10	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1704701C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600574C	FDA UDI	Class II	Active
Implant Prosthetics	8000620	FDA UDI	Class II	Active
Shiner Magnet System	1421404	FDA UDI	Class II	Active
Implant Prosthetics	8001485	FDA UDI	Class II	Active
Equator	2144443	FDA UDI	Class II	Active
Preat Implant Prosthetics	0604068	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600402C	FDA UDI	Class II	Active
Implant Prosthetics	8003470	FDA UDI	Class II	Active
Implant Prosthetics	9000675	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600906C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606704C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006875	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006652	FDA UDI	Class I	Active
Implant Prosthetics	9001650-10	FDA UDI	Class II	Unknown
Zimmer	8000189	FDA UDI	Class II	Active
Implant Prosthetics	8000852	FDA UDI	Class II	Active
Implant Prosthetics	8000981	FDA UDI	Class II	Active
Astra	8006761	FDA UDI	Class II	Active
Ackermann	0102124	FDA UDI	Class I	Active
Sphero Attachments	0814402	FDA UDI	Class II	Active
Shiner Magnet System	1400014	FDA UDI	Class I	Unknown
Implant Prosthetics	8000676	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605406	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005645	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600204C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605702C	FDA UDI	Class II	Active
Sphero Attachments	0819650	FDA UDI	Class II	Active
Preci-Bar	0101111	FDA UDI	Class I	Unknown
Implant Prosthetics	8005080	FDA UDI	Class II	Active
Implant Prosthetics	8001571	FDA UDI	Class II	Active
Implant Prosthetics	9000500-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8003721	FDA UDI	Class II	Active
Sphero Attachments	0803070	FDA UDI	Class II	Active
Sphero Attachments	0819802	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600805C	FDA UDI	Class II	Active
Implant Prosthetics	8003480	FDA UDI	Class II	Active
Straumann	8001441	FDA UDI	Class I	Active
Branemark	8004176	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600813C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9003724	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600553C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006869	FDA UDI	Class II	Active
Implant Prosthetics	9005832-10	FDA UDI	Class II	Unknown
Zimmer	8000310	FDA UDI	Class I	Active
Sphero Attachment	0809102	FDA UDI	Class II	Active
Fiber Technology	7009060-5	FDA UDI	Class II	Unknown
Preat Implant Driver Tools	9000037	FDA UDI	Class I	Active
O-Ring	1701601	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.