FDA Device Intelligence
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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

Recent recalls

DateFirmReason
2015-02-11EXP Pharmaceutical Services CorpEXP 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
2011-12-09Progressive Medical IncSome of the sterile packages had broken seals.
2011-10-28Progressive Medical IncThe tip of the product could come loose or unravel.
2010-03-01He, IncSterile product packaging contains weak seals, which may result in compromised product sterility.
2008-08-08Sterilmed IncSteriMed, 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
2007-11-06Ethicon Endo-Surgery IncSterility (package integrity) compromised; Damaged packaging may have compromised the sterility of the devices.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.