LifeScience PLUS, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000004095 FEI 3004957256
LifeScience PLUS, Inc. is a medical device manufacturer based in the United States, with 37 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Unclassified and Class I; EU Class III) as of 13 Nov 2026.
- Devices
- 37
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 28
- EUDAMED 5
- FDA 510(k) 4
- Device classes
- FDA Unclassified 30
- EU Class III 5
- FDA Class I 2
- Top EMDN categories
- Sites and related companies
- Wellkang Ltd authorised representative
- Identifiers
- EUDAMED SRN US-MF-000004095
- FDA FEI 3004957256
- DUNS 190600051
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- Wellkang LtdXI
Catalogue
Search and filter all 37 devicesCompany details
- EUDAMED SRN
- US-MF-000004095
- FDA FEI number
- 3004957256
- DUNS number
- 190600051
- EUDAMED status
- Active
- EUDAMED registered name
- LifeScience PLUS, Inc.
- EUDAMED abbreviated name
- LSP
- Registered address
- 2520A, Wyandotte St., 94043, Mountain View, United States
- Website
- www.lifescienceplus.com
- facebook.com/lifescienceplus
- Phone
- +1 6505658172
- PRRC contact
- Deborah Hurley
From the company website
LifeScience PLUS is a leader in advanced wound care technology. We are committed to developing and marketing innovative total wound care solutions: hemostasis (bleeding control), sealant, moist dressing, contamination prevention, and fast tissue growth generation. Our patented, best-in-class flagship product—BloodSTOP® iX Advanced Hemostat with WoundHEAL®—utilizes our game-changing technology for both acute and chronic wound care.
Frequently asked questions
How many devices does LifeScience PLUS, Inc. have in the registry?
The registry currently lists 37 devices for LifeScience PLUS, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LifeScience PLUS, Inc.'s devices?
Among its 37 most recently registered devices, LifeScience PLUS, Inc. has devices listed in EUDAMED (5 devices), FDA 510(k) (4 devices) and FDA GUDID (28 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LifeScience PLUS, Inc.'s devices fall under?
Among its 37 most recently registered devices, the classes recorded for LifeScience PLUS, Inc.'s devices are Class I and Class III. Each device page shows its own class and authorisation.
What are the newest devices from LifeScience PLUS, Inc. in the registry?
The most recently registered devices listed for LifeScience PLUS, Inc. include BloodSTOP iX Trauma Seal TS-iX-26, Trauma Seal TS-iX-37, BloodSTOP 832230 and BloodSTOP iX BS-iX-14N.