Product code NBL— Dental
C50
- Classification name
- Light-Induced Fluorescence Caries Detector
- Device class
- Class 2
- Regulation
- 21 CFR 872.1745
- Advisory panel
- Dental
- Total cleared
- 24
- First cleared
- Most recent
Market context for product code NBL
FDA has cleared devices under product code NBL between 2000 and 2026, filed by 18 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2026
- 2025
- 2024
- 2023
- 2022
- 2020
- 2018
- 2017
- 2016
- 2013
- 2012
- 2011
- 2010
- 2009
- 2007
Top applicants under product code NBL
Recent clearances under product code NBL
- K252464 — Surgical Microscope (OMS2360, OMS2380)
- K242103 — TRIOS Ready Tip
- K221275 — Qraycam PRO
- K231722 — SmarTooth
- K223470 — C50
- K221249 — L1P-1F (TRIOS 5)
- K183471 — IC-WHCD100 (Inspire)
- K171007 — Fluorescence Mode
- K170822 — Electronic Caries Detector
- K150672 — VistaCam iX Proof
- K121685 — SOPROCARE
- K112139 — THE CANARY SYSTEM
- K111423 — CS 1600 INTRAORAL CAMERA
- K111321 — REMOTE VIEW SOFTWARE
- K093705 — FUORECAM
- K092583 — SOPROLIFE
- K090598 — CARIESCAN PRO
- K090169 — SPECTRA FLUORESCENCE CARIES DETECTION DEVICE
- K063321 — D-CARIE/DETECTAR, MODELS N121, N123, N133, N134, N135 & N138
- K051909 — DIAGNODENT
- K042394 — DIAGNODENT PERIO TIP (ACCESSORY)
- K043156 — D-CARIE, MODEL N121-M1
- K040063 — INSPEKTOR PRO
- DEN990002 — KAVO DIAGNODENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.