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TAS Medical, Inc.

United StatesFDA 510(k) applicant, unverified FDA FEI 3029835193

Devices
11
Registrations
FDA
FDA recalls
11 ongoing

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI, FDA recalls

Catalogue11

Newest first, rows 1-11 of 11

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Rows 1-11 of 11

Company details

FDA FEI number
3029835193
DUNS number
111249727
Address
9100 Conroy Windermere Rd, Windermere, FL, 34786

FDA recalls1

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

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 1
  • 2026 0
  • 2025

    • 27 Jan 2025 Z-1294-2025 Class II Ongoing Tissue approximation straps (zip-ties) have broken before or during implantation so firm developed an interim zip-tie conditioning method submerging zip-ties in 104-degrees F sterile saline solution for 60 min prior to implantation to rehydrate the zip-tie straps. Broken zip-ties not observed during procedure could lead to future hernia recurrence, recurrent surgery to correct a large herniation. Distribution: US Nationwide distribution in the states of LA, OK, TN. Submission number: K220980

Frequently asked questions

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

The registry currently lists 11 devices for TAS Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

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

Among its 11 most recently registered devices, TAS Medical, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 11 most recently registered devices, the classes recorded for TAS Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

FDA recall records list 1 recall initiated by TAS Medical, Inc., the most recent initiated on 2025-01-27. 1 of them is recorded as ongoing. 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 TAS Medical, Inc. in the registry?

The most recently registered devices listed for TAS Medical, Inc. include TAS Medical, Inc. Tissue Approximation System T-5000, TAS Medical, Inc. Tissue Approximation System T-LAP, Tissue Approximation System and TAS Medical, Inc. Tissue Approximation System T-4000.

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