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Sontec Instruments, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1720747

Devices
14,543
Registrations
FDA
FDA recalls
0

What Sontec Instruments, Inc. makes

SONTEC Instruments, Inc. manufactures reusable surgical instruments, including needle holders, general-purpose scissors, soft-tissue manipulation forceps (tweezers-like and scissors-like variants), orthopaedic rongeurs, bone curettes, retractors, and ophthalmic forceps. Their product line also includes specialized tools like the Lester Lens Pusher, Jacobson Scissors, and Desmarres Lid Retractor, as well as urological and corneal forceps.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue14,543

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Company details

FDA FEI number
1720747
Address
7248 S Tucson Way, CENTENNIAL, CO, 80112

Frequently asked questions

How many devices does SONTEC INSTRUMENTS, INC. have in the registry?

The registry currently lists 14543 devices for SONTEC INSTRUMENTS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SONTEC INSTRUMENTS, INC.'s devices?

Among its 50 most recently registered devices, SONTEC INSTRUMENTS, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do SONTEC INSTRUMENTS, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for SONTEC INSTRUMENTS, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from SONTEC INSTRUMENTS, INC. in the registry?

The most recently registered devices listed for SONTEC INSTRUMENTS, INC. include Micro Osteotome 475-7864, Laparoscopic Bulldog Clamp 2901-281-45, Laparoscopic Bulldog Clamp 2901-281-60 and Yankauer Pediatric Suction Tube 180-446.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.