FDA device listing

CMOS Video Rhino-Laryngoscope SSU

FDA device listing 1770293496 · Kunststoff Helmbrechts AG

Key facts

Proprietary names CMOS Video Rhino-Laryngoscope SSU
Owner/operator Kunststoff Helmbrechts AG
Owner/operator number 10059824
Product codes EOB
Device names EOB - Nasopharyngoscope (Flexible Or Rigid)
Device class Class II
Classification regulations (21 CFR) 874.4760
Review panels Ear, Nose, & Throat
Registered establishments KH Czechia s.r.o., KUNSTSTOFF HELMBRECHTS AG
Establishment registrations 3008439484, 3015925378
FEI numbers 3008439484, 3015925378
Establishment operations Contract Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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