Origin Medsystems, Inc.
FDA 510(k) medical device clearances.
Top product codes for Origin Medsystems, Inc.
Recent clearances by Origin Medsystems, Inc.
- K992353 — BLUNT TIP TROCAR PORT
- K981700 — VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM
- K972685 — ORIGIN LIGATOR DEVICE
- K970611 — ORIGIN CARDIAC STABLIZER OCCLUDER
- K965121 — CANNULA
- K964171 — VASOVIEW BALLOON DISSECTION SYSTEM
- K962104 — AIRLIFT BALLOON RETRACTON SYSTEM
- K962005 — EXTRAHAND BALLOON RETRACTOR
- K960936 — RESPOSABLE TROCAR SYSTEM [5MM, 5MM SHORT, 10MM AND 12MM SIZES]
- K960637 — 5MM ENDOSCOPE
- K955163 — DISSECTION PROBE
- K954174 — DUO BALLOON SYSTEM (DBS) 2 [10 AND 12 MM SIZES]
- K954175 — DUO BALLOON SYSTEM (DBS) 1[10 AND 12 MM SIZES]
- K953377 — DISTENTION BALLOON
- K953561 — PREPERITONEAL DISTENTION BALLOON SYSTEMS (MODIFICATION)
- K946002 — ORIGIN PREPERITONEAL DISSECTION BALLOON SYSTEM (PDBS)--EXTRA
- K944415 — ORIGIN TACKER SYSTEM
- K945023 — ORIGIN PIXIE STIC INTRODUCER SLEEVE
- K944304 — ORIGIN BALLOON ANCHOR
- K942678 — LIFTING DISTENTION BALLOON SYSTEM
- K942491 — ORIGIN BALLOON RETRACTOR
- K942636 — PSB PREPERITONEAL STRUCTURE BALLOON
- K940875 — ADJUSTABLE BALLOON DISSECTION CANNULA
- K930813 — PISTOL SUCTION/IRRIGATION PROBE
- K930848 — SENSING TIP SURGICAL TROCAR
- K931522 — FASCIAL CLOSURE DEVICE
- K933075 — LAPAROSCOPIC RETRACTOR
- K935426 — PREPERITONEAL DISTENTION BALLOON SYSTEM
- K933724 — SENSOR-TIP TROCAR
- K933106 — ENDOSCOPE
- K926480 — LAPAROSCOPIC BALLOON RETRACTOR
- K934134 — DISTENTION INSTRUMENT, MODIFICATION
- K921103 — RETRACTION INSTRUMENT
- K932229 — SURGICAL TROCAR AND TROCAR SLEEVE
- K924011 — ORIGIN BLUNT TIP SURGICAL TROCAR
- K930301 — TROCAR SHEATH ANCHOR
- K922094 — DISSECTION INSTRUMENT
- K921040 — ENDOSCOPE
- K922751 — ORIGIN FLEXIBLE PORT
- K922460 — ORIGIN SECONDARY CANNULA AND TROCAR
- K920599 — HOOK SURGICAL INSTRUMENT
- K915116 — TROCAR SHEATH ANCHOR
- K913816 — ORIGINEEDLE, MODIFICATION
- K914203 — LAPAROSCOPIC BALLOON RETRACTOR
- K904848 — PORT-OF-ORGIN(TM) SINGLE-USE TROCAR AND SLEEVE
- K904849 — ORIGINEEDLE(TM)
- K904156 — ORIGIN(TM) CEMENT EXTRACT SYST STD-PR/SPL-PR KITS
- K904180 — PROSTHETIC CEMENT REMOVER
- K890989 — DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR
- K896584 — ARTHROSCOPIC TUBING SHEATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.