FDA device listing

2.0mm Drill Bit,3.0mm Drill Bit

FDA device listing 1525904506 · Precision Edge Surgical Products Company

Key facts

Proprietary names 2.0mm Drill Bit,3.0mm Drill Bit
Owner/operator Precision Edge Surgical Products Company
Owner/operator number 10042577
Product codes JDR
Device names JDR - Staple, Fixation, Bone
Device class Class II
Classification regulations (21 CFR) 888.3030
Review panels Orthopedic
Registered establishments PRECISION EDGE SURGICAL PRODUCTS COMPANY
Establishment registrations 1833986
FEI numbers 1000139987
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

Browse all FDA device listings