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ACTEON

SATELEC · Model KIT TIPS CE PZT 2 · UDI-DI 03609820875545

DZI Prescription
1
510(k) clearances
1,060
Adverse events
20
Recalls
80
Facilities

Description

CROWN EXTENSION KIT: Completely innocuous to the gingiva guaranteeing the integrity of bone and adjacent teeth. A tip for each stage: the instrument sequence adapts to the different surgical crown lengthening stages, starting from extensive bone remodeling up to precise osteotomy.

Recalls

DateFirmReason
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r
2019-03-14Nobel Biocare Usa LlcDue to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall r

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.