Home › Device types › GDI
Dissector, Surgical, General & Plastic Surgery
FDA product code GDI · Class 1 · General, Plastic Surgery
1,968
Registered devices
307
Adverse events
6
Recalls
7
510(k) clearances
Devices with this code
Gimmi — Gimmi GmbHIllico — ALPHATEC SPINE, INC.Hayden Medical — Hayden Medical, Inc.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftLAZIC — Peter Lazic GmbHMillennium — Avalign Technologies, Inc.Wexler Surgical, Inc. — WEXLER SURGICAL, INC.Hayden Medical — Hayden Medical, Inc.Symmetry Surgical Rapidclean® MARYLAND — ASPEN SURGICAL PRODUCTS, INC.KYPHON® Introducer Tool Kit — MEDTRONIC SOFAMOR DANEK, INC.DeRoyal — DEROYAL INDUSTRIES, INC.Symmetry Rhoton® — ASPEN SURGICAL PRODUCTS, INC.Dissector — KOROS U.S.A., INC.AESCULAP — Aesculap AGN/A — BIOMET MICROFIXATION, INCGen2 — SURGIX MEDICAL LLCGimmi — Gimmi GmbHIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONLAZIC — Peter Lazic GmbHPILLING — TELEFLEX INCORPORATEDMIASPAS MINI-TTA — Aesculap AGAESCULAP — Aesculap AGDissector — KOROS U.S.A., INC.Wexler Surgical, Inc. — WEXLER SURGICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-11 | EXP Pharmaceutical Services Corp | EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that |
| 2011-12-09 | Progressive Medical Inc | Some of the sterile packages had broken seals. |
| 2011-10-28 | Progressive Medical Inc | The tip of the product could come loose or unravel. |
| 2010-03-01 | He, Inc | Sterile product packaging contains weak seals, which may result in compromised product sterility. |
| 2008-08-08 | Sterilmed Inc | SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted becau |
| 2007-11-06 | Ethicon Endo-Surgery Inc | Sterility (package integrity) compromised; Damaged packaging may have compromised the sterility of the devices. |
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