510(k) K210711

Neocis Guidance System (NGS) with Yomi Plan v2.0.1 by Neocis, Inc. — Product Code PLV

K210711 is an FDA 510(k) premarket notification submitted by Neocis, Inc. for the device "Neocis Guidance System (NGS) with Yomi Plan v2.0.1". The FDA issued a decision of Substantially Equivalent on December 22, 2021. The device falls under product code PLV (Dental Stereotaxic Instrument), a Class II device regulated under 21 CFR 872.4120. Neocis, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 2021
Date Received
March 10, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dental Stereotaxic Instrument
Device Class
Class II
Regulation Number
872.4120
Review Panel
DE
Submission Type

To facilitate dental implant placement in patients that are partially endentulous or edentulous.