FDA device listing

NC Variobase Abutment with screw, D 3.8mm, H 3.5mm, TAN,NNC Variobase Abutment, with screw, D 5.05mm, H 4mm, TAN,RC…

FDA device listing 1050801990 · INSTITUT STRAUMANN AG

Key facts

Proprietary names NC Variobase Abutment with screw, D 3.8mm, H 3.5mm, TAN,NNC Variobase Abutment, with screw, D 5.05mm, H 4mm, TAN,RC Variobase Abutment, with screw, D 4.5mm, 3.5mm, TAN,RN Variobase Abutment, with screw, D 5.05mm, H 4mm, TAN,WN Variobase Abutment, with screw, D 7mm, H 4.5mm, TAN
Owner/operator INSTITUT STRAUMANN AG
Owner/operator number 9005052
Premarket submissions K142890
Product codes NHA
Device names NHA - Abutment, Implant, Dental, Endosseous
Device class Class II
Classification regulations (21 CFR) 872.3630
Review panels Dental
Registered establishments etkon GMBH, INSTITUT STRAUMANN AG, Straumann Manufacturing, Inc., Straumann Villeret SA
Establishment registrations 9613348, 9614404, 3011221537, 3024185724, 3033781108
FEI numbers 3002807318, 3004975279, 3011221537, 3024185724, 3033781108
Establishment operations Contract Manufacturer, Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 10–99 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes 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

Browse all FDA device listings