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.
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