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510(k) K210947

Navident by Claronav, Inc. — Product Code PLV

K210947 is an FDA 510(k) premarket notification submitted by Claronav, Inc. for the device "Navident". The FDA issued a decision of Substantially Equivalent on June 27, 2022. The device falls under product code PLV (Dental Stereotaxic Instrument), a Class II device regulated under 21 CFR 872.4120. Claronav, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 27, 2022
Date Received
March 30, 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.

Other clearances by Claronav, Inc.

  • K243053 — Navient Image Guided Navigation System (ENT) (955-NC-NC) (June 20, 2025)
  • K241327 — Navient Image Guide Navigation System (955-NC-NC), Cranial (February 5, 2025)
  • K233563 — Navident (July 25, 2024)
  • K163439 — NaviENT (September 1, 2017)
  • K161406 — Navident (September 8, 2016)

Other clearances for product code PLV

  • K252376 — Yomi S Robotic System (October 28, 2025)
  • K251835 — Yomi Robotic System (October 10, 2025)
  • K233563 — Navident (July 25, 2024)
  • K231018 — Yomi Robotic System (August 14, 2023)
  • K211466 — Yomi Robotic System with YomiPlan Go (June 14, 2022)
  • K213392 — INLIANT Surgical Navigation System (February 22, 2022)
  • K210711 — Neocis Guidance System (NGS) with Yomi Plan v2.0.1 (December 22, 2021)
  • K211129 — Neocis Guidance System (NGS) with Intraoral Fiducial Array (July 28, 2021)
  • K203401 — Neocis Guidance System (NGS) with Patient Splints (EPS) (December 15, 2020)
  • K202264 — Neocis Guidance System (NGS) with Yomi Plan v2.0 (December 4, 2020)

FDA data resources