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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 6 of 80

Device	Model / Reference	Registries	Class	Status
Sphero Attachments	0819828	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605905C	FDA UDI	Class II	Active
Preat	9005165	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705806C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007161	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605403C	FDA UDI	Class II	Active
Preat	9005168	FDA UDI	Class II	Active
Implant Prosthetics	9000503-10	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1500243	FDA UDI	Class II	Unknown
Astra®-compatible	8002040	FDA UDI	Class I	Unknown
Implant Prosthetics	8003760	FDA UDI	Class II	Unknown
Implant Prosthetics	8002820	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608004C	FDA UDI	Class II	Active
Implant Prosthetics	8001577	FDA UDI	Class II	Active
Astra	8006462	FDA UDI	Class II	Active
Implant Prosthetics	9004932	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1600506C	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006835	FDA UDI	Class II	Active
Implant Prosthetics	8001083	FDA UDI	Class II	Active
Implant Prosthetics	9000830-10	FDA UDI	Class I	Unknown
O-Ring Implant Abutments	1500247	FDA UDI	Class II	Unknown
Fiber Technology	7009011-2	FDA UDI	Class II	Unknown
O-Ring	1700904	FDA UDI	Class II	Active
Sphero Attachments	0812220	FDA UDI	Class II	Active
Implant Prosthetics	8004478	FDA UDI	Class II	Active
Preat	0800196	FDA UDI	Class I	Active
Preat	9003759	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007545	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005830	FDA UDI	Class II	Active
Implant Prosthetics	8003385	FDA UDI	Class II	Active
Preat	710713	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000845	FDA UDI	Class I	Active
Preat Implant Prosthetics	9007152	FDA UDI	Class I	Active
Implant Prosthetics	9001500-10	FDA UDI	Class I	Unknown
Preat	3694C29	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1600503	FDA UDI	Class II	Active
Hiossen	8005121	FDA UDI	Class II	Active
Preat	2RT00H1	FDA UDI	Class I	Active
Implant Prosthetics	9003732-100	FDA UDI	Class II	Unknown
Preat	9000100	FDA UDI	Class I	Active
Preat Implant Prosthetics	1605801C	FDA UDI	Class II	Active
Ceka	3ZCS230	FDA UDI	Class II	Active
Preat	9005565	FDA UDI	Class II	Active
Preat	1500197	FDA UDI	Class I	Active
Preat	0808705	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006701	FDA UDI	Class I	Active
Implant Prosthetics	9000950-10	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600806C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1706802C	FDA UDI	Class II	Active
Preat	7551705	FDA UDI	Class I	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.