Renaissance Pharmaceutical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Renaissance Pharmaceutical, Inc. makes
The company produces sterile wound hydrogel dressings designed for topical application to wounds, including those requiring moist wound healing environments. These products are formulated to absorb excess exudate while maintaining a hydrated wound bed, supporting tissue repair and reducing the risk of infection.
The portfolio consists of Class II (U) devices authorised via the FDA’s 510(k) pathway. These products are listed under the FDA’s regulatory framework and are intended for use in the United States.
Catalogue
Wound Hydrogel And/Or Sterile Wound Hydrogel Ref K961316
Regimes: 510(k) Registry: 510(k)Wound Hydrogel And/Or Sterile Wound Hydrogel Ref K954384
Regimes: 510(k) Registry: 510(k)Wound Hydrogel & Sterile Wound Hydrogel Ref K961766
Regimes: 510(k) Registry: 510(k)Sterile Wound Hydrogel Dressing Ref K941339
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Renaissance Pharmaceutical, Inc. have in the registry?
The registry currently lists 4 devices for Renaissance Pharmaceutical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renaissance Pharmaceutical, Inc.'s devices?
Among its 4 most recently registered devices, Renaissance Pharmaceutical, Inc. has devices listed in FDA 510(k) (4 devices).
What are the newest devices from Renaissance Pharmaceutical, Inc. in the registry?
The most recently registered devices listed for Renaissance Pharmaceutical, Inc. include WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL, WOUND HYDROGEL & STERILE WOUND HYDROGEL and STERILE WOUND HYDROGEL DRESSING.