R-Med, Inc.

FDA Regulatory Profile

R-Med, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 17, 2000.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001236RIZA BAND STRETCHER (RBS)-60000July 17, 2000
K953360R-MED ABDOMINAL WALL ELEVATORJanuary 11, 1996
K954882RIZA-RIBE NEEDLE (MODIFICATION)November 16, 1995
K953441RIZA-RIBE NEEDLEAugust 18, 1995
K950108R-MED MINI-RETRACTORMay 11, 1995
K942411R-MED DISPOSABLE PLUGMarch 31, 1995
K945637R-MED MOTORIZED LAPAROSCOPIC HANDLEDecember 7, 1994
K943818MANUAL LAPAROSOPIC HANDLE, INTERCHANGEABLE LAPAROSCOPIC TOOL UNITSAugust 29, 1994
K935031RIZA-RIBE NEEDLEApril 25, 1994