ClearanceBrief
Company ยท US

Johnson & Johnson Consumer, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2018. Name variants (Inc, Corp, punctuation) are merged.

2510(k) clearances (0 in 12 months)
6recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FQMBandage, Elastic6
OHSLight Based Over The Counter Wrinkle Reduction1
OLPOver-The-Counter Powered Light Based Laser For Acne1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 19, 2018K180856Neutrogena Light Therapy Aging Mask+
Johnson & Johnson Consumer, Inc.
OHS
Jun 19, 2018K180847Neutrogena Light Therapy Acne Mask+
Johnson & Johnson Consumer, Inc.
OLP

Latest recalls

DateFirm and productCodeLinked 510(k)
Mar 27, 2018Johnson & Johnson Consumer, Inc.
Johnson & Johnson BAND-AID Brand First Aid Products HURT-FREE Wrap (size: 2in)
Terminated
FQMNone listed
Mar 27, 2018Johnson & Johnson Consumer, Inc.
Johnson & Johnson BAND-AID Brand First Aid Products HURT-FREE Wrap (size: 1in)
Terminated
FQMNone listed
Mar 27, 2018Johnson & Johnson Consumer, Inc.
Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 3in)
Terminated
FQMNone listed
Mar 27, 2018Johnson & Johnson Consumer, Inc.
Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 2in)
Terminated
FQMNone listed
Mar 27, 2018Johnson & Johnson Consumer, Inc.
COACH Self-Adhering Sports Wrap (size: 3in)
Terminated
FQMNone listed
Mar 27, 2018Johnson & Johnson Consumer, Inc.
COACH Self-Adhering Sports Wrap (size: 2in)
Terminated
FQMNone listed
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