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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 70 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	8005050	FDA UDI	Class II	Unknown
O-Ring Implant Abutments	1600804C	FDA UDI	Class II	Active
Implant Prosthetics	9000951	FDA UDI	Class I	Active
Implant Prosthetics	8003757	FDA UDI	Class II	Unknown
Implant Prosthetics	9004932-100	FDA UDI	Class II	Unknown
Implant Prosthetics	9001550-10	FDA UDI	Class I	Unknown
Implant Prosthetics	8003757-10	FDA UDI	Class II	Unknown
Implant Prosthetics	8001575	FDA UDI	Class II	Active
FR Attachments	0702040	FDA UDI	Class I	Active
Nobel	8000490	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9001945	FDA UDI	Class I	Active
Preat	9000662	FDA UDI	Class II	Active
Preat	2RP0065	FDA UDI	Class I	Active
Implant Prosthetics	8004850	FDA UDI	Class II	Active
Implant Prosthetics	9000677	FDA UDI	Class II	Active
Implant Prosthetics	9000432-50	FDA UDI	Class I	Unknown
Zimmer	8000106	FDA UDI	Class I	Active
Preat	0101375-2	FDA UDI	Class I	Active
Preat	9000054	FDA UDI	Class I	Active
Preat	30285NP	FDA UDI	Class I	Active
Implant Prosthetics	9004175	FDA UDI	Class II	Active
Preat	0808925	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600574	FDA UDI	Class II	Unknown
Implant Prosthetics	8001550	FDA UDI	Class II	Unknown
Preci-Bar	0101107	FDA UDI	Class I	Unknown
Preat	7551615	FDA UDI	Class I	Unknown
Preat	9001563	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600301C	FDA UDI	Class II	Active
Implant Prosthetics	8000550-10	FDA UDI	Class II	Unknown
Camlog	8003230	FDA UDI	Class II	Active
Preat	0819436	FDA UDI	Class II	Active
Preat	9000695	FDA UDI	Class II	Active
Sphero Flex	0828613	FDA UDI	Class II	Active
eFiber	7009052	FDA UDI	Class II	Active
Implant Prosthetics	9004454	FDA UDI	Class II	Active
Implant Prosthetics	9000303	FDA UDI	Class I	Active
O-Ring Implant Abutments	1600823C	FDA UDI	Class II	Active
Preat	9005653	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006722	FDA UDI	Class II	Active
Sphero Attachments	0800751	FDA UDI	Class II	Active
Astra®-compatible	8002041	FDA UDI	Class I	Active
Preat	9001790	FDA UDI	Class II	Active
Implant Prosthetics	9000935	FDA UDI	Class II	Active
Preat Implant Prosthetics	9007264	FDA UDI	Class II	Active
Preat	9002253	FDA UDI	Class II	Active
Preat Implant Prosthetics	1707002C	FDA UDI	Class II	Active
eFiber	7009050	FDA UDI	Class II	Unknown
Preat	710162	FDA UDI	Class II	Active
Preat	9001265-F	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006663	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.