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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 59 of 80

Device	Model / Reference	Registries	Class	Status
Clix Ball Implant Abutments	1600305C	FDA UDI	Class II	Active
Implant Prosthetics	8001870	FDA UDI	Class II	Active
Equator	2149506	FDA UDI	Class II	Active
Sphero Attachment	0823076	FDA UDI	Class II	Active
Sphero Attachments	0811403	FDA UDI	Class II	Active
Implant Prosthetics	8003576	FDA UDI	Class II	Active
Preat	9000581	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608003	FDA UDI	Class II	Active
Preat	9000569	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006761	FDA UDI	Class II	Active
Implant Prosthetics	9006700-25	FDA UDI	Class I	Unknown
Implant Prosthetics	9001200	FDA UDI	Class I	Active
Implant Prosthetics	8000977	FDA UDI	Class II	Active
Implant Prosthetics	9001881	FDA UDI	Class II	Active
Hader	0101770	FDA UDI	Class I	Active
Implant Prosthetics	8002720	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1601401C	FDA UDI	Class II	Active
Preat	0101236	FDA UDI	Class I	Active
Hader Bar	0101750	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601704C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605803C	FDA UDI	Class II	Active
Implant Prosthetics	8001059	FDA UDI	Class II	Active
Implant Prosthetics	9001700	FDA UDI	Class I	Active
O-Ring Implant Abutments	1600803	FDA UDI	Class II	Active
O-Ring	1700602	FDA UDI	Class II	Active
Implant Prosthetics	9000580	FDA UDI	Class II	Active
Hader	0101705	FDA UDI	Class I	Active
Implant Prosthetics	8001779	FDA UDI	Class II	Active
Preat	9006790	FDA UDI	Class II	Active
Sphero Block	0811407	FDA UDI	Class II	Active
Preat	0101251B	FDA UDI	Class I	Active
Implant Prosthetics	8004863	FDA UDI	Class II	Active
Implant Prosthetics	8001671	FDA UDI	Class II	Active
Preat	8003705	FDA UDI	Class I	Active
O-Ring	1700573	FDA UDI	Class II	Active
Implant Prosthetics	9001232-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9000135-25	FDA UDI	Class I	Unknown
Sphero Attachment	0803794	FDA UDI	Class II	Active
Preat	9005435	FDA UDI	Class II	Unknown
Branemark	8001010	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007100	FDA UDI	Class I	Active
3i Certain	8001915	FDA UDI	Class I	Active
Preat Implant Prosthetics	9006424	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600201	FDA UDI	Class I	Unknown
Clix Ball Implant Abutments	1600601C	FDA UDI	Class II	Active
Implant Prosthetics	8002275	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007262	FDA UDI	Class II	Active
Implant Prosthetics	9007132	FDA UDI	Class II	Unknown
Implant Prosthetics	9001554	FDA UDI	Class II	Active
Implant Prosthetics	8004762	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.