Skip to content

Taut, Inc.

United StatesFDA applicant, unverified

Devices
16
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue16

Newest first, rows 1-16 of 16

Search and filter all 16 devices
Skip device list

Rows 1-16 of 16

FDA recalls1

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

  • 2007

    • 19 Jan 2007 Z-0428-2007 Unclassified (pre-2012) Terminated Taut, Inc. has become aware that some package seals are not intact, compromising the sterility of the catheters. Distribution: Worldwide, including USA, Guam, Australia, Iceland and Italy Submission number: K960883

Frequently asked questions

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

The registry currently lists 16 devices for Taut, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Taut, Inc.'s devices?

Among its 16 most recently registered devices, Taut, Inc. has devices listed in FDA 510(k) (16 devices).

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

Among its 16 most recently registered devices, the classes recorded for Taut, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Taut, Inc.?

FDA recall records list 1 recall initiated by Taut, Inc., the most recent initiated on 2007-01-19. 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 Taut, Inc. in the registry?

The most recently registered devices listed for Taut, Inc. include O.P.C. INTRAVASCULAR CATHETER, TAUT BALLOON CATHETER, MODEL 50640, TUAT SPLATTER CONTROL SHIELD SCS-300 and ADAPT OPEN ACCESS PORT, MODEL 41233.

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