FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Medworks Corp.
Medworks Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K982630
MEDWORKS VISUALIZATION INSEMINATION CATHETER
January 14, 1999
K982628
MEDWORKS INSEMINATION CATHETER
August 21, 1998
K982626
URETHROPEXY SUTURE PLACEMENT KIT MODEL NUMBERS UM-300, MW-100, MINI-LAPAROTOMY MMK KIT MODEL UM-250,
August 20, 1998