FDA device listing

Curette, Operative

FDA device listing 1841754224 · Young Innovations Inc

Key facts

Owner/operator Young Innovations Inc
Owner/operator number 9046427
Product codes EKE
Device names EKE - Curette, Operative
Device class Class I
Classification regulations (21 CFR) 872.4565
Review panels Dental
Registered establishments SALVIN DENTAL SPECIALTIES, LLC
Establishment registrations 1066741
FEI numbers 3003005156
Establishment operations Repackager/Relabeler
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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