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510(k) K242600

Second Opinion Periapical Radiolucency Contours by Pearl, Inc. — Product Code MYN

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 11, 2025
Date Received
August 30, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Medical Image
Device Class
Class II
Regulation Number
892.2070
Review Panel
RA
Submission Type

For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers

Other clearances by Pearl, Inc.

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  • K243989 — Second Opinion® 3D (May 23, 2025)
  • K243230 — Second Opinion® BLE (May 9, 2025)
  • K243893 — Second Opinion® Pediatric (May 5, 2025)
  • K242522 — Second Opinion CC (January 16, 2025)
  • K210365 — Second Opinion (March 4, 2022)

Other clearances for product code MYN

  • K251934 — qXR-Detect (January 16, 2026)
  • K252934 — Diagnocat (January 15, 2026)
  • K253009 — DS Core Detect (January 7, 2026)
  • K252086 — DTX Studio Assist (November 17, 2025)
  • K250525 — Second Opinion® Panoramic (November 14, 2025)
  • K250264 — SugarBug (1.x) (November 7, 2025)
  • K251002 — Videa Dental AI (September 19, 2025)
  • K250753 — VELMENI for DENTISTS (V4D) (September 2, 2025)
  • K243234 — Second Opinion® CS (June 12, 2025)
  • K242437 — Smile Dx® (May 14, 2025)