Covalontechnologies, Inc.

FDA Regulatory Profile

Covalontechnologies, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 14, 2017.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K163556MediClear PreOpSeptember 14, 2017
K150550SilverCoat Silicone Foley CatheterNovember 24, 2015
K121819SURGICLEAR ANTIMICROBIAL CLEAR SILICONE ADHESIVE DRESSING WITH CHLORHEXIDINE AND SILVERAugust 13, 2012
K112549IV CLEAR ANTIMICROBIAL CLEAR SILICONE ADHESIVE DRESSING WITH CHLORHEXIDINE AND SILVERMay 4, 2012
K043296COLACTIVE AG COLLAGEN WITH SILVER ANTIMICROBIAL DRESSINGJune 6, 2005
K050177COLACTIVE COLLAGEN WOUND DRESSINGApril 27, 2005