FDA device listing

VERSALOK ANCHOR WITH FREE STRANDS OF ORTHOCORD SUTURE (210808), ETHIBOND SUTURE (210809), AND PANACRYL SUTURE (210810)

FDA device listing 2047164804 · Exel Inc. dba DHL Supply Chain (USA)

Key facts

Proprietary names VERSALOK ANCHOR WITH FREE STRANDS OF ORTHOCORD SUTURE (210808), ETHIBOND SUTURE (210809), AND PANACRYL SUTURE (210810)
Owner/operator Exel Inc. dba DHL Supply Chain (USA)
Owner/operator number 10026656
Premarket submissions K063478
Product codes GAM, GAS, GAT, HWC, MBI, NEW
Device names GAM - Suture, Absorbable, Synthetic, Polyglycolic Acid, GAS - Suture, Nonabsorbable, Synthetic, Polyester, GAT - Suture, Nonabsorbable, Synthetic, Polyethylene, HWC - Screw, Fixation, Bone, MBI - Fastener, Fixation, Nondegradable, Soft Tissue, NEW - Suture, Surgical, Absorbable, Polydioxanone
Device class Class II
Classification regulations (21 CFR) 878.4493, 878.4840, 878.5000, 888.3040
Review panels General & Plastic Surgery, Orthopedic
Registered establishments EXEL INC. DBA DHL SUPPLY CHAIN (USA)
Establishment registrations 3008868758
FEI numbers 3008868758
Establishment operations Repackager/Relabeler
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes 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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