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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 54 of 80

Device	Model / Reference	Registries	Class	Status
Preat	0809633	FDA UDI	Class II	Active
O-Ring	1705405	FDA UDI	Class II	Active
Implant Prosthetics	9000230-10	FDA UDI	Class I	Unknown
Sphero Attachment	0818651	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608005C	FDA UDI	Class II	Active
Preat	2R165TI	FDA UDI	Class I	Active
Gingivamoll	0906412	FDA UDI	Class I	Unknown
Implant Prosthetics	8001259	FDA UDI	Class II	Unknown
Nobel	8000404	FDA UDI	Class I	Active
Preat	20144AE	FDA UDI	Class I	Active
Preat	9001935	FDA UDI	Class II	Active
Preci 52	0101561	FDA UDI	Class I	Active
Preat	0822765	FDA UDI	Class II	Active
Shiner Magnet System	1400165	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9003721	FDA UDI	Class II	Active
Implant Prosthetics	9005000-10	FDA UDI	Class I	Unknown
O-Ring	1705406	FDA UDI	Class II	Active
Preat	9000268	FDA UDI	Class II	Active
Direct	8000080	FDA UDI	Class I	Active
Sphero Attachments	0819553	FDA UDI	Class II	Active
Implant Prosthetics	8003476	FDA UDI	Class II	Active
Hiossen® HG-compatible	8005140	FDA UDI	Class I	Unknown
Implant Prosthetics	9000480	FDA UDI	Class II	Active
Preat Implant Prosthetics	1607002C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600554C	FDA UDI	Class II	Active
Preat	2192ECE	FDA UDI	Class I	Active
Preat	0818771	FDA UDI	Class II	Active
Preat	1500607	FDA UDI	Class I	Active
O-Ring	1700601	FDA UDI	Class II	Active
Implant Prosthetics	9001478	FDA UDI	Class II	Active
Sphero Attachments	0809634	FDA UDI	Class II	Active
Preat	0800161	FDA UDI	Class I	Active
Preat Implant Prosthetics	8004961	FDA UDI	Class II	Active
Sphero Attachments	0801001	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	9007268	FDA UDI	Class II	Active
Implant Prosthetics	9000676	FDA UDI	Class II	Active
Preat	9006453	FDA UDI	Class II	Active
Preat	9004153	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007045	FDA UDI	Class I	Active
MegaGen	8004410	FDA UDI	Class I	Active
Preat	1500532	FDA UDI	Class I	Active
Preat	0803301	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000230	FDA UDI	Class II	Active
Implant Prosthetics	9004450-10	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600202	FDA UDI	Class II	Unknown
Astra	8006859	FDA UDI	Class II	Active
Sphero Attachments	0801002	FDA UDI	Class II	Active
Preat	0807500	FDA UDI	Class I	Active
Astra	8002110	FDA UDI	Class I	Active
Preat	9002259	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.