Data / Medical devices / United States / Lifescience Plus, Inc.
Lifescience Plus, Inc.: FDA-registered device maker in Mountain View, CA, United States, 4 510(k) clearances
Lifescience Plus, Inc. is registered with the FDA (registration 3004957256) in Mountain View, CA, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated April 30, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004957256
- Address
- 2520-A Wyandotte Street, Mountain View, CA, United States, 94043
- Owner or operator
- LIFESCIENCE PLUS, INC. (9069203)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- November 7, 2007
- Registered through
- 2027
- Brand names listed
- WoundFlex
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Compression | MHW | 1 | Manufacturer | accessdata.fda.gov |
| Hemostatic Wound Dressing Without Thrombin Or Other Biologics | QSY | U | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 30, 2026 | K253017 | BloodSTOP iX Trauma Matrix (TM-iX-20) | QSY | Substantially Equivalent | Lifescience Plus, Inc. | accessdata.fda.gov |
| June 29, 2016 | K160130 | BloodSTOP iX Battle Matrix | QSY | Substantially Equivalent | Lifescience Plus, Inc. | accessdata.fda.gov |
| November 2, 2007 | K072681 | BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE | QSY | Substantially Equivalent | Lifescience Plus, Inc. | accessdata.fda.gov |
| September 27, 2007 | K071578 | BLOODSTOP AND BLOODSTOP IX HEMOSTATIC GAUZE, MODELS BS-10,BS-11,BS-12,B-13, BS-IX27, BS-IX-14, BSIX-15, BSIX-17 | QSY | Substantially Equivalent | Lifescience Plus, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Hemostatic Wound Dressing Without Thrombin Or Other Biologics
- All makers of Dressing, Compression
Updated April 30, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.