FDA device listing

Fiber Optic Rod

FDA device listing 1521209720 · SCHOTT CR, s.r.o.

Key facts

Proprietary names Fiber Optic Rod
Owner/operator SCHOTT CR, s.r.o.
Owner/operator number 10025265
Product codes EBZ
Device names EBZ - Activator, Ultraviolet, For Polymerization
Device class Class II
Classification regulations (21 CFR) 872.6070
Review panels Dental
Registered establishments SCHOTT CR, S.R.O.
Establishment registrations 3006984716
FEI numbers 3006984716
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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