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Mini Lap Technologies, Inc.

United StatesFDA applicant, unverified

Devices
7

What Mini Lap Technologies, Inc. makes

Mini Lap Technologies, Inc. manufactures surgical instruments for minimally invasive procedures, including electrocautery devices, retractors, and pediatric-specific tools with a Medusa clamping system. Their portfolio also includes reusable needleoscopic devices and bipolar electrocautery instruments designed for precision in laparoscopic surgeries.

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are based in the United States and appear in the FDA’s 510(k) registry.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Mini Lap Technologies, Inc. have in the registry?

The registry currently lists 7 devices for Mini Lap Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mini Lap Technologies, Inc.'s devices?

Among its 7 most recently registered devices, Mini Lap Technologies, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Mini Lap Technologies, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Mini Lap Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mini Lap Technologies, Inc. in the registry?

The most recently registered devices listed for Mini Lap Technologies, Inc. include MINI LAP ELECTROCAUTERY INSTRUMENTS, MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM, MINI LAP INSTRUMENTS and MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM.

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