Hemostasis, LLC - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Hemostasis, LLC has 10 FDA 510(k) cleared general & plastic surgery devices. Based in St. Paul, US.
Latest FDA clearance: Jul 2024. Active since 2007.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hemostasis, LLC
10 devices
Cleared
Jul 26, 2024
Resolv Endoscopic Hemostat System
General & Plastic Surgery
211d
Cleared
Nov 14, 2022
PosiSep X BAM Hemostat Dressing/Intranasal Splint
Ear, Nose, Throat
283d
Cleared
May 05, 2022
PosiSep EAR Fragmentable Ear Dressing
Ear, Nose, Throat
448d
Cleared
Jan 23, 2015
OsteoSeal Bone Hemostat
General & Plastic Surgery
154d
Cleared
Mar 27, 2013
POSISEP AND POSISEP X HEMOSTAT DRESSING/INTRANASAL SPLINT
Ear, Nose, Throat
223d
Cleared
Nov 15, 2012
NEXSTAT PLUS AND NEXFOAM PLUS TOPICAL HEMOSTAT DRESSING
General & Plastic Surgery
56d
Cleared
Jul 25, 2012
POSISEP AND POSISEP X HEMOSTAT DRESSINGS
General & Plastic Surgery
117d
Cleared
Dec 03, 2010
NEXSTAT (TM) TOPICAL HEMOSTAT POWDER
General & Plastic Surgery
98d
Cleared
Oct 26, 2007
EXCELARREST FOAM
General & Plastic Surgery
15d
Cleared
Apr 05, 2007
TRAUMARREST AND BLEEDARREST HEMOSTATIC PARTICLES AND FOAM
General & Plastic Surgery
73d