FDA device listing

DISPOSABLE SCISSORS,MEDICAL

FDA device listing 1806664963 · AESCULAP CHIFA SP. Z O. O.

Key facts

Proprietary names DISPOSABLE SCISSORS,MEDICAL
Owner/operator AESCULAP CHIFA SP. Z O. O.
Owner/operator number 9007699
Product codes JOK
Device names JOK - Scissors, Medical, Disposable
Device class Class I
Classification regulations (21 CFR) 880.6820
Review panels General Hospital
Registered establishments AESCULAP CHIFA SP. Z O.O.
Establishment registrations 9680260
FEI numbers 3002315844
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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