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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 46 of 80

Device	Model / Reference	Registries	Class	Status
Implant Prosthetics	9002200	FDA UDI	Class I	Active
Implant Prosthetics	9003730-100	FDA UDI	Class II	Unknown
Implant Prosthetics	8000285	FDA UDI	Class II	Active
Preat Implant Prosthetics	1605902C	FDA UDI	Class II	Active
Sphero Attachment	0801005	FDA UDI	Class II	Active
Implant Prosthetics	9001600-10	FDA UDI	Class I	Unknown
Ackermann	0102119	FDA UDI	Class I	Active
Preat	0700006	FDA UDI	Class I	Active
Preat	1500214	FDA UDI	Class I	Unknown
Hader Bar	0101775	FDA UDI	Class I	Active
Preat	9004969	FDA UDI	Class II	Active
Implant Prosthetics	8005159	FDA UDI	Class II	Active
Equator	2148118	FDA UDI	Class II	Active
Hader	0101755	FDA UDI	Class I	Active
Clix Ball Implant Abutments	1601506	FDA UDI	Class II	Active
Implant Prosthetics	9005176	FDA UDI	Class II	Active
Sphero Attachments	0819023	FDA UDI	Class II	Active
Implant Prosthetics	9006732-50	FDA UDI	Class II	Unknown
O-Ring	1700505	FDA UDI	Class II	Active
Camlog	8003200	FDA UDI	Class I	Active
Equator	2142792	FDA UDI	Class II	Active
O-Ring	1700553	FDA UDI	Class II	Active
Preat	3X691DP	FDA UDI	Class I	Active
Shiner Magnet System	1400010	FDA UDI	Class I	Unknown
Implant Prosthetics	8005062	FDA UDI	Class II	Unknown
Preat	0829170	FDA UDI	Class II	Active
Preat Implant Prosthetics	1606602C	FDA UDI	Class II	Active
Implant Prosthetics	8003573	FDA UDI	Class II	Active
Implant Prosthetics	9000835-10	FDA UDI	Class I	Unknown
Fiber Technology	7009070-3	FDA UDI	Class II	Unknown
Implant Prosthetics	9000150	FDA UDI	Class II	Unknown
Clix Ball Implant Abutments	1608006C	FDA UDI	Class II	Active
Preat Implant Prosthetics	1705701C	FDA UDI	Class II	Active
Preat	01K1265	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	1602001C	FDA UDI	Class I	Unknown
Shiner Magnet System	1400011	FDA UDI	Class I	Unknown
Preat Implant Prosthetics	9001535	FDA UDI	Class II	Active
Zimmer	8000123	FDA UDI	Class II	Active
Preat	7551305	FDA UDI	Class I	Unknown
Preat	2RT0H14	FDA UDI	Class I	Active
Stick®	7009072	FDA UDI	Class I	Active
Preat	0800280	FDA UDI	Class I	Active
Preat	0822673	FDA UDI	Class II	Active
Sphero Attachment	0812002	FDA UDI	Class II	Active
Clix Ball Implant Abutments	1608002	FDA UDI	Class II	Active
Preat	9004461	FDA UDI	Class II	Active
Preat Implant Prosthetics	1600553	FDA UDI	Class II	Unknown
Implant Prosthetics	8003750-10	FDA UDI	Class II	Unknown
Preat	0809632	FDA UDI	Class II	Active
Preci-Bar	0101109	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.