ClearanceBrief
Company ยท US

Inamed Development Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1994. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered3
FFPDilator, Rectal1
FZWExpander, Surgical, Skin Graft1
GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered1
KGOSurgeon'S Gloves1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 10, 1994K931548INAMED DEVELOPMENT ASPIRATION TIP
Inamed Development Co.
GCX
Mar 6, 1991K904265INAMED RUIZ-COHEN INTRAOPERATIVE TISSUE EXPANDER
Inamed Development Co.
FZW
May 7, 1990K901764INAMED CONVERTIBLE DRAIN SYSTEM
Inamed Development Co.
GCY
May 7, 1990K901742INAMED SMALL DRAIN SYSTEM
Inamed Development Co.
GCY
Jan 18, 1990K894618INAMED RHEMO-D (TM) DILATOR
Inamed Development Co.
FFP
Jan 8, 1990K896491INAMED CLOSED-WOUND DRAIN SYSTEM
Inamed Development Co.
GCY
Sep 18, 1989K894073INAMED PRO-TEC SILICONE SURGICAL GLOVES
Inamed Development Co.
KGO

Latest recalls

DateFirm and productCodeLinked 510(k)
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