Skip to content

Greenwald Surgical Co., Inc.

United StatesFDA applicant, unverified

Devices
4

What Greenwald Surgical Co., Inc. makes

Greenwald Surgical Co., Inc. manufactures flexible endoscopic electrodes for precision tissue ablation, including cystoscopic and ureteroscopic variants with controlled tip designs. Their product line also includes a Baumrucker clamp for incontinence management, designed for surgical use in urological procedures.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) database. Their products are listed under US jurisdiction, adhering to applicable medical device regulations.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

Frequently asked questions

How many devices does Greenwald Surgical Co., Inc. have in the registry?

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

Which registries list Greenwald Surgical Co., Inc.'s devices?

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

What risk classes do Greenwald Surgical Co., Inc.'s devices fall under?

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

What are the newest devices from Greenwald Surgical Co., Inc. in the registry?

The most recently registered devices listed for Greenwald Surgical Co., Inc. include GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE, GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE, CLAMP, INCONTINENCE, BAUMRUCKER and GREENWALD CONTROL TIP URETEROSCOPIC ELECTRODE.

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