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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 30 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9000481	FDA UDI	Class II	Active
Implant Prosthetics	8001973	FDA UDI	Class II	Active
Implant Prosthetics	9001677	FDA UDI	Class II	Active
CAMLOG® Screw-Line-compatible	8003241	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007063	FDA UDI	Class II	Active
Preat	710213	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600576	FDA UDI	Class II	Unknown
Sphero Flex	0828682	FDA UDI	Class II	Active
Implant Prosthetics	9003700-10	FDA UDI	Class I	Unknown
O-Ring	1701204	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601505C	FDA UDI	Class II	Active
Nobel Active	8004735	FDA UDI	Class II	Active
Preci Profile	0101410	FDA UDI	Class I	Unknown
Preat	30295TI	FDA UDI	Class I	Active
Implant Prosthetics	9004189	FDA UDI	Class II	Active
Implant Prosthetics	9005730	FDA UDI	Class II	Unknown
Ankylos®-compatible	8004841	FDA UDI	Class I	Active
Implant Prosthetics	8000581	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005822	FDA UDI	Class II	Active
Implant Prosthetics	9007132-50	FDA UDI	Class II	Unknown
Implant Prosthetics	9002189	FDA UDI	Class II	Active
Implant Prosthetics	8000976	FDA UDI	Class II	Active
Sphero Attachments	0829422	FDA UDI	Class II	Active
Implant Prosthetics	8005061	FDA UDI	Class II	Active
Preat	0101751	FDA UDI	Class I	Active
Preat	0808698	FDA UDI	Class I	Active
Preat	1400336	FDA UDI	Class I	Unknown
O-Ring	1600821	FDA UDI	Class II	Active
Implant Prosthetics	8000589	FDA UDI	Class II	Active
Preat	9000861	FDA UDI	Class II	Active
Implant Prosthetics	8001470	FDA UDI	Class II	Active
Branemark	8004178	FDA UDI	Class II	Unknown
Preat	1100005	FDA UDI	Class I	Active
Preat	0819550	FDA UDI	Class II	Active
Preat	0803807	FDA UDI	Class II	Active
Preat	9005095	FDA UDI	Class II	Active
Implant Prosthetics	9002181	FDA UDI	Class II	Active
Preat	9005665-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9003760-100	FDA UDI	Class II	Active
Preat	7551320	FDA UDI	Class I	Unknown
Implant Prosthetics	8005077	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000867-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9001503	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005767-F	FDA UDI	Class II	Active
Preat	9001665	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706404C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006677	FDA UDI	Class II	Active
O-Ring	1500502-6	FDA UDI	Class I	Unknown
Shiner Magnet System	1421403	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600812	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.