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Conmed Endoscopic Technologies, Inc.

United StatesFDA applicant, unverified

Devices
2
FDA recalls
15

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue2

Newest first, rows 1-2 of 2

FDA recalls15

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Showing the 10 most recent of 15 recalls.

  • 2007

    • 16 Apr 2007 Z-0937-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0938-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0939-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0940-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0941-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0942-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0943-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0944-2007 Unclassified (pre-2012) Terminated Complaints received regarding PET Balloon Dilators for a variety of labeling errors, including: incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0945-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0946-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
Show all 15 recalls

  • 2007

    • 16 Apr 2007 Z-0947-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0948-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 16 Apr 2007 Z-0949-2007 Unclassified (pre-2012) Terminated Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator. Distribution: Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the…
      Full distribution text Worldwide-Devices distributed to medical facilities and distributors Nationwide (USA) and to distributors in the following countries: Australia, Belgium, Canada, Croatia, Denmark, Germany, India, Italy, Japan, Mexico, Poland, Spain and Sweden.
      Submission number: K033936
    • 14 Mar 2007 Z-0729-2007 Unclassified (pre-2012) Terminated Blue safety clip incorrectly placed on the stent may prevent deployment Distribution: Worldwide distribution, USA including states of DE, OH, MI, DC and countries of Belgium Japan. Submission number: K031186
    • 14 Mar 2007 Z-0730-2007 Unclassified (pre-2012) Terminated Blue safety clip incorrectly placed on the stent may prevent deployment Distribution: Worldwide distribution, USA including states of DE, OH, MI, DC and countries of Belgium Japan. Submission number: K031186

Frequently asked questions

How many devices does Conmed Endoscopic Technologies, Inc. have in the registry?

The registry currently lists 2 devices for Conmed Endoscopic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Conmed Endoscopic Technologies, Inc.'s devices?

Among its 2 most recently registered devices, Conmed Endoscopic Technologies, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Conmed Endoscopic Technologies, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Conmed Endoscopic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Conmed Endoscopic Technologies, Inc.?

FDA recall records list 15 recalls initiated by Conmed Endoscopic Technologies, Inc., the most recent initiated on 16 Apr 2007. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Conmed Endoscopic Technologies, Inc. in the registry?

The most recently registered devices listed for Conmed Endoscopic Technologies, Inc. include DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996, 000997, 000998 and CONMED AXCESS PAPILLOTOME MODELS AX4535, AX4535FX.

Generated automatically from registry data and not verified by a human reviewer.