FDA device listing

AL701008,AL701020,ASIM20640012,ASIM22312,ASIM22512, ASIM22712, ASIM22517, ASIM29515…

FDA device listing 1775225674 · ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.

Key facts

Proprietary names AL701008,AL701020,ASIM20640012,ASIM22312,ASIM22512, ASIM22712, ASIM22517, ASIM29515, ASSI.MTK22512,ASIM23859CC,ASIM24015,ASIM24315,ASIM24826,ASIM25326,ASIM25626,ASIM26326,ASIM27326,ASIM2891,ASIM5111, ASIM5212, ASIM5214, ASIM5311, ASIM5312, ASIM5511, ASIM5711,ASIM54826,ASIM6111, ASIM6212, ASIM6214, ASIM6311, ASIM6312, ASIM6511…
Owner/operator ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.
Owner/operator number 2434839
Product codes GEN
Device names GEN - Forceps, General & Plastic Surgery
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP.
Establishment registrations 2434839
FEI numbers 2434839
Establishment operations Contract 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