FDA device listing

BONE SCREW RULER,Steel Ruler

FDA device listing 1640940842 · Aristotech Industries GmbH

Key facts

Proprietary names BONE SCREW RULER,Steel Ruler
Owner/operator Aristotech Industries GmbH
Owner/operator number 10053573
Product codes FTY
Device names FTY - Tape, Measuring, Rulers And Calipers
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments Aristotech Industries GmbH
Establishment registrations 3014314623
FEI numbers 3014314623
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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