BloodSTOP iX Trauma Matrix (TM-iX-20)
K-Number: K253017 · 2026-04-30
Device Summary
Frequently Asked Questions
What is the BloodSTOP iX Trauma Matrix (TM-iX-20)?
BloodSTOP iX Trauma Matrix (TM-iX-20) is a medical device that received FDA 510(k) clearance on 2026-04-30. The listed applicant is Lifescience Plus, Inc.. The 510(k) number is K253017.
When did BloodSTOP iX Trauma Matrix (TM-iX-20) receive FDA 510(k) clearance?
BloodSTOP iX Trauma Matrix (TM-iX-20) received FDA 510(k) clearance on 2026-04-30, under 510(k) number K253017.
Who is the listed applicant for BloodSTOP iX Trauma Matrix (TM-iX-20)?
The FDA 510(k) record lists Lifescience Plus, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BloodSTOP iX Trauma Matrix (TM-iX-20)?
The FDA product code for BloodSTOP iX Trauma Matrix (TM-iX-20) is QSY.
Other records listing Lifescience Plus, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QSY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.