Renaissance Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Renaissance Medical, Inc. makes
Renaissance Medical, Inc. produces sterile wound hydrogels and hydrogel-based dressings, including single-dose units, for topical application to wounds. These products are designed to maintain a moist wound environment to support healing.
The company’s portfolio is classified under Class II (U) devices in the US and is listed in the FDA’s 510(k) registry. Products are regulated under the US Food and Drug Administration’s medical device authorities.
Catalogue
Wound Hydrogel And/Or Sterile Wound Hydrogel Ref K935203
Regimes: 510(k) Registry: 510(k)Royl-Derm Wound Hydrogel Sterile Unit Dose Ref K933817
Regimes: 510(k) Registry: 510(k)Royl-Derm Wound Hydrogel Ref K922815
Regimes: 510(k) Registry: 510(k)Royl-Derm Wound Hydrogel Dressing Ref K932973
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Renaissance Medical, Inc. have in the registry?
The registry currently lists 4 devices for Renaissance Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renaissance Medical, Inc.'s devices?
Among its 4 most recently registered devices, Renaissance Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What are the newest devices from Renaissance Medical, Inc. in the registry?
The most recently registered devices listed for Renaissance Medical, Inc. include WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL, ROYL-DERM WOUND HYDROGEL STERILE UNIT DOSE, ROYL-DERM WOUND HYDROGEL and ROYL-DERM WOUND HYDROGEL DRESSING.