Home › Device types › GDI
Dissector, Surgical, General & Plastic Surgery
FDA product code GDI · Class 1 · General, Plastic Surgery
1,963
Registered devices
307
Adverse events
6
Recalls
7
510(k) clearances
Devices with this code
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHPMI — PROGRESSIVE MEDICAL, INC.LAZIC — Peter Lazic GmbHLife Instruments — Life Instrument CorporationLife Instruments — Life Instrument CorporationAmbler Surgical — AMBLER SURGICAL CORP.HNM MEDICAL — HNM STAINLESS, LLC.Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC.Symmetry Surgical Rapidclean® MIXTER — ASPEN SURGICAL PRODUCTS, INC.ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONMarina Medical — MARINA MEDICAL INSTRUMENTS, INC.gSource — GSOURCE LLCKMEDIC — TELEFLEX INCORPORATEDN/A — BIOMET MICROFIXATION, INCGimmi — Gimmi GmbHNA — DEPUY SPINE, LLCRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftAmbler Surgical — AMBLER SURGICAL CORP.American Medicals — American MedicalsMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftAESCULAP — Aesculap AGMSI Precision Specialty Instruments — Med Saver, Inc.Life Instruments — Life Instrument Corporation
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
