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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 69 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9005459	FDA UDI	Class II	Active
Implant Prosthetics	8000582	FDA UDI	Class II	Active
Hader	0101703	FDA UDI	Class I	Active
Implant Prosthetics	8005170	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600814	FDA UDI	Class II	Active
Preat	9005253	FDA UDI	Class II	Active
Sphero Attachment	0813071	FDA UDI	Class II	Active
Fiber Technology	7009011-6	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1706704C	FDA UDI	Class II	Active
Equator	2144435	FDA UDI	Class II	Active
Preat	9005059	FDA UDI	Class II	Active
Implant Prosthetics	9004421	FDA UDI	Class II	Active
Implant Prosthetics	8000559	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005924	FDA UDI	Class II	Active
Preat	7551200	FDA UDI	Class I	Unknown
Implant Prosthetics	9005177	FDA UDI	Class II	Active
Implant Prosthetics	9003730-50	FDA UDI	Class II	Unknown
Hader Bar	0101704-6	FDA UDI	Class I	Active
Preat	2R175IR	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600106	FDA UDI	Class II	Active
Implant Prosthetics	9000300	FDA UDI	Class I	Active
Implant Prosthetics	9000550-10	FDA UDI	Class I	Unknown
Sphero Attachments	0800514	FDA UDI	Class II	Active
Equator	2149801	FDA UDI	Class II	Active
Preat	0101820	FDA UDI	Class I	Active
Preat	9001668	FDA UDI	Class II	Active
O-Ring Implant Abutments	1600824C	FDA UDI	Class II	Active
O-Ring	1700506	FDA UDI	Class II	Active
Preat	9004159	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007200	FDA UDI	Class I	Active
Preat	2141915	FDA UDI	Class II	Active
Preci-Sagix	0101311-6	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600403C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006723	FDA UDI	Class II	Active
Preat	9005895	FDA UDI	Class II	Active
Implant Prosthetics	9001267	FDA UDI	Class II	Active
Preat Implant Prosthetics	1604702C	FDA UDI	Class II	Active
Implant Prosthetics	9004432	FDA UDI	Class II	Unknown
Equator	2142005	FDA UDI	Class II	Active
Preat	9006865	FDA UDI	Class II	Active
Preat	9005565-F	FDA UDI	Class II	Active
Preat	9005751	FDA UDI	Class I	Active
Implant Prosthetics	8000962	FDA UDI	Class II	Unknown
Nobel	8000610	FDA UDI	Class I	Active
Preat	1400600	FDA UDI	Class I	Unknown
Preat	0814302	FDA UDI	Class II	Active
Preat	2R185TI	FDA UDI	Class I	Active
Implant Prosthetics	9001830-10	FDA UDI	Class II	Unknown
Preat	9005030	FDA UDI	Class II	Active
Implant Prosthetics	9001450	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.