FDA device listing

123-105 TONO/051-048-12S TC NEEDLE HOLDERS HEGAR BAUMGARTNER 12 CM,123-106 TONO/051-048-14S TC NEEDLE HOLDERS HEAGR…

FDA device listing 1945146705 · Avilign Medical

Key facts

Proprietary names 123-105 TONO/051-048-12S TC NEEDLE HOLDERS HEGAR BAUMGARTNER 12 CM,123-106 TONO/051-048-14S TC NEEDLE HOLDERS HEAGR BAUMGARTNER 14 CM,123-130 TONO/051-060-15S TC NEEDLE HOLDERS CRILEWOOD 15 CM,123-131 TONO/051-060-18S TC NEEDLE HOLDERS CRILEWOOD 18 CM,123-132 TONO/051-060-20S TC NEEDLE HOLDERS CRILEWOOD 20 CM,123-135 TONO/051-080-16S TC NEEDLE HOLDERS MAYO HEGAR 16 CM,123-140 TONO/051-080-18S TC…
Owner/operator Avilign Medical
Owner/operator number 10053881
Product codes MDM
Device names MDM - Instrument, Manual, Surgical, General Use
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments AVILIGN MEDICAL
Establishment registrations 3012226300
FEI numbers 3012226300
Establishment operations Contract Manufacturer, Manufacturer, 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

Browse all FDA device listings