Den Med, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Den Med, Inc. makes
Den Med, Inc. manufactures non-sterile and sterile gauze sponges, which are absorbent cotton pads used for wound care, surgical applications, and medical cleaning.
The company’s gauze sponges are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The products are intended for use in the United States.
Catalogue
Gauze Sponge-Non-Sterile Sponge Ref K831182
Regimes: 510(k) Registry: 510(k)Gauze Sponge Sterile Sponge Ref K831183
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Den Med, Inc. have in the registry?
The registry currently lists 2 devices for Den Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Den Med, Inc.'s devices?
Among its 2 most recently registered devices, Den Med, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Den Med, Inc. in the registry?
The most recently registered devices listed for Den Med, Inc. include GAUZE SPONGE-NON-STERILE SPONGE and GAUZE SPONGE STERILE SPONGE.