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Tnco, Inc.

United StatesFDA applicant, unverified

Devices
4
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Tnco, Inc. makes

Tnco, Inc. manufactures endoscopic surgical instruments, including monopolar surgical tools and arthroscopic surgical instruments. Their portfolio includes monopolar endoscopic reusable tip surgical instruments designed for minimally invasive procedures.

These devices are classified as Class II under FDA regulations and are recorded in the 510(k) premarket notification process. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

FDA recalls1

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

FDA recall records list 1 recall initiated by Tnco, Inc., initiated on 2005-12-02. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2005

    • 2 Dec 2005 Z-0434-06 Unclassified (pre-2012) Terminated The tip may not engage with the handle and may dislodge Distribution: CA, CT, DC, IL, IN, FL. GA, NC, NY, UT Canada Submission number: K943958

Frequently asked questions

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

The registry currently lists 4 devices for Tnco, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tnco, Inc.'s devices?

Among its 4 most recently registered devices, Tnco, Inc. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for Tnco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Tnco, Inc.?

FDA recall records list 1 recall initiated by Tnco, Inc., the most recent initiated on 2 Dec 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 Tnco, Inc. in the registry?

The most recently registered devices listed for Tnco, Inc. include ENDOSCOPIC SURGICAL INSTRUMENTS, MONOPOLAR SURGICAL INSTRUMENTS, TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS and MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS.

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