Bioartificial Gel Technologies (Bagtech), Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Bioartificial Gel Technologies (Bagtech), Inc. makes
Bioartificial Gel Technologies produces sterile, hydrogel-based wound dressings, including the BIOAQUACARE (Model C-10 in multiple sizes) with and without gauze, packaged in blister packs or plastic bags. It also manufactures the RADIO BIOAQUACARE, a variant designed for radiated wound care.
These products are classified as Class II (U) devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Radio Bioaquacare Ref K080471
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioartificial Gel Technologies (Bagtech), Inc. have in the registry?
The registry currently lists 2 devices for Bioartificial Gel Technologies (Bagtech), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioartificial Gel Technologies (Bagtech), Inc.'s devices?
Among its 2 most recently registered devices, Bioartificial Gel Technologies (Bagtech), Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Bioartificial Gel Technologies (Bagtech), Inc. in the registry?
The most recently registered devices listed for Bioartificial Gel Technologies (Bagtech), Inc. include BIOAQUACARE, MODEL C-10( VARIOUS SIZES) WITH AND WITHOUT GAUZE, BLISTER PACKAGED OR IN PLASTIC BAG CONTAINERS and RADIO BIOAQUACARE.