Skip to content

Tissuelink Medical, Inc.

United StatesFDA applicant, unverified

Devices
12
FDA recalls
3

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue12

Newest first, rows 1-12 of 12

Search and filter all 12 devices
Skip device list

Rows 1-12 of 12

FDA recalls3

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2005

    • 7 Feb 2005 Z-0563-05 Unclassified (pre-2012) Terminated The tip may separate from the device and render it unusable Distribution: AZ, CA, CO, CT, DE, IL, FL, KS, KY, OH, MA, MD MO,NC, NY, PA, RI, SC, TN,TX, VA Foreign: Italy, Turkey, Egypt, Spain,…
      Full distribution text AZ, CA, CO, CT, DE, IL, FL, KS, KY, OH, MA, MD MO,NC, NY, PA, RI, SC, TN,TX, VA Foreign: Italy, Turkey, Egypt, Spain, Peru, Portugal, Australia, Netherlands Government: VA Medical Center 508 Fulton Street Durham, NC 27005 VA Medical Center- 7400 Merton Minter Blvd San Antonio, TX 78229 VA Medical Center- Pittsburgh University C Pittsburgh, PA 15240
      Submission number: K014260

  • 2004

    • 22 Jul 2004 Z-1415-04 Unclassified (pre-2012) Terminated Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing. Distribution: Nationwide Submission numbers: K020574, K022532
    • 22 Jul 2004 Z-1416-04 Unclassified (pre-2012) Terminated Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing. Distribution: Nationwide Submission numbers: K020574, K022532

Frequently asked questions

How many devices does Tissuelink Medical, Inc. have in the registry?

The registry currently lists 12 devices for Tissuelink Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tissuelink Medical, Inc.'s devices?

Among its 12 most recently registered devices, Tissuelink Medical, Inc. has devices listed in FDA 510(k) (12 devices).

What risk classes do Tissuelink Medical, Inc.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Tissuelink Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Tissuelink Medical, Inc.?

FDA recall records list 3 recalls initiated by Tissuelink Medical, Inc., the most recent initiated on 7 Feb 2005. 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 Tissuelink Medical, Inc. in the registry?

The most recently registered devices listed for Tissuelink Medical, Inc. include TISSUELINK AQUAMANTYS MALLEABLE BIPOLAR SEALER WITH LIGHT, TISSUELINK BIPOLAR FORCEPS, TISSUELINK BIPOLAR FLOATING BALL DEVICE and MODIFICATION TO TISSUELINK BIPOLAR FORCEPS.

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