Orthoconcept, Inc.

FDA Regulatory Profile

Orthoconcept, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 17, 1994.

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925160ARTHRO FMS 4February 17, 1994
K910164ORTHOCONCEPT ARTHROSCOPIC PUMPMarch 27, 1991
K905785ARTHRO-FMS-3/IRRIGATION SETS (VARIOUS)March 26, 1991
K896196ARTHROSCOPY DISP. & REUSABLE SHAVER BLADES, RECHARDecember 1, 1989
K895643MODIFIED UROPUMP* FLUID MANAGEMENT SYSTEMOctober 17, 1989
K894363UROPUMP* FLUID MANAGEMENT SYSTEMAugust 11, 1989
K882469CORDEX SHAVER, BLADES, RECHARGER AND BATTERIESDecember 1, 1988
K872270ORTHOCONCEPT ARTHROSCOPIC PUMP ORTHOPUMPJuly 21, 1987