ClearanceBrief
Company ยท US

Andover Healthcare Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2009. Name variants (Inc, Corp, punctuation) are merged.

1510(k) clearances (0 in 12 months)
7recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FQMBandage, Elastic7
FRODressing, Wound, Drug1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 30, 2009K083133SILVERI: COFLEX AFD, COFLEX AFD FIRST AID, AFD PAD FOAM DRESSING, POWERFLEX AFD FOAM DRESSINGS
Andover Healthcare, Inc.
FRO

Latest recalls

DateFirm and productCodeLinked 510(k)
May 15, 2024Andover Healthcare Inc.
Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage, Tan, 4INx5YD (5400S)
Open, Classified
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Terminated
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Terminated
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Terminated
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Terminated
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Terminated
FQMNone listed
Jun 19, 2019Andover Healthcare Inc.
Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Terminated
FQMNone listed
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