FDA device listing

Driver (Fixture Driver, Screw Driver, Hand Driver, Solid Driver),Fixture Mount (IHFMM35, IHFMR37, IHFMR40),IH FIXTURE…

FDA device listing 1686506726 · Sewon Medix, Inc.

Key facts

Proprietary names Driver (Fixture Driver, Screw Driver, Hand Driver, Solid Driver),Fixture Mount (IHFMM35, IHFMR37, IHFMR40),IH FIXTURE LAB ANALOG(IHFLAM120, IHFLAR120, IHFLAR120D, IHFLAM150, IHFLAR150, IHFLAR150D),IH IMPRESSION COPING(AIHPIMH4011, AIHPIMH4015, IHPIMH4511, IHPIMH4515, AIHPIRH4511, AIHPIRH4515),IH IMPRESSION COPING(AIHPIMN4011, AIHPIMN4015, IHPIMN4511, IHPIMN4515, AIHPIRN4511, AIHPIRN4515),IH…
Owner/operator Sewon Medix, Inc.
Owner/operator number 10053110
Product codes NDP
Device names NDP - Accessories, Implant, Dental, Endosseous
Device class Class I
Classification regulations (21 CFR) 872.3980
Review panels Dental
Registered establishments SEWON MEDIX, INC.
Establishment registrations 3013271380
FEI numbers 3013271380
Establishment operations 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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