FDA device listing

CISION Disposable Surgical Scalpel

FDA device listing 1447133869 · Ag Marketing & Development Group Inc Dba Agmd Group

Key facts

Proprietary names CISION Disposable Surgical Scalpel
Owner/operator Ag Marketing & Development Group Inc Dba Agmd Group
Owner/operator number 10089735
Product codes GES
Device names GES - Blade, Scalpel
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP
Establishment registrations 3016844398
FEI numbers 3016844398
Establishment operations Foreign Exporter
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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