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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 4 of 80

Device	Model / Reference	Registries	Class	Status
Clix Ball Implant Abutments	1601404C	FDA UDI	Class II	Active
Preat Implant Prosthetics	0802427	FDA UDI	Class II	Active
Branemark	8001030	FDA UDI	Class II	Active
FR Attachments	0702010	FDA UDI	Class I	Active
Implant Prosthetics	9001435	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005445	FDA UDI	Class I	Active
Sphero Attachment	0809950	FDA UDI	Class II	Active
Neoss	8004162	FDA UDI	Class II	Unknown
Straumann	8001337	FDA UDI	Class II	Active
Preat	1600035	FDA UDI	Class I	Active
Hader	0101737	FDA UDI	Class I	Active
Preat	9003765	FDA UDI	Class II	Active
Preat	9000965-F	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1600905	FDA UDI	Class II	Active
Preat Implant Prosthetics	9006769	FDA UDI	Class II	Active
Preci-Sagix	0101359	FDA UDI	Class I	Active
Preat	9000468	FDA UDI	Class II	Active
Preat Implant Prosthetics	9005878	FDA UDI	Class II	Active
Preat	9001762	FDA UDI	Class II	Active
Preat Implant Prosthetics	9000903	FDA UDI	Class I	Active
Preat	9000868	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605301C	FDA UDI	Class I	Unknown
Implant Prosthetics	9006450	FDA UDI	Class II	Active
Implant Prosthetics	9000330	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9005704	FDA UDI	Class I	Active
Legacy-compatible	9008503	FDA UDI	Class I	Active
Preat	2RP0085	FDA UDI	Class I	Active
Preat Implant Prosthetics	9005869	FDA UDI	Class II	Active
Preat Implant Prosthetics	9003760-HL	FDA UDI	Class II	Unknown
Preat	244CAIN	FDA UDI	Class I	Active
Implant Prosthetics	9005410	FDA UDI	Class II	Unknown
Implant Prosthetics	9003732-50	FDA UDI	Class II	Unknown
Implant Prosthetics	9001600-25	FDA UDI	Class I	Unknown
Implant Prosthetics	8000670	FDA UDI	Class II	Active
Sphero Attachment	0801401	FDA UDI	Class II	Active
Implant Prosthetics	8004857	FDA UDI	Class II	Active
Preat	0800250	FDA UDI	Class I	Active
Nobel	8000851	FDA UDI	Class I	Unknown
Gingivamoll	0906409	FDA UDI	Class I	Unknown
Preat	7551405	FDA UDI	Class I	Unknown
Fiber Technology	7009007	FDA UDI	Class II	Unknown
Preat Implant Prosthetics	1600202	FDA UDI	Class II	Active
Preat	9000664	FDA UDI	Class II	Active
Preat	7551750	FDA UDI	Class I	Unknown
Preat	710083	FDA UDI	Class II	Active
Preat	50000-55	FDA UDI	Class II	Unknown
Preat	7551600	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9006754	FDA UDI	Class II	Active
Preat	9003742	FDA UDI	Class I	Active
Preat Implant Prosthetics	9000145	FDA UDI	Class I	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.