ClearanceBrief
Company ยท US

Aesthetic and Reconstructive Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2003. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MIBElastomer, Silicone Block4
FWPProsthesis, Chin, Internal1
FZEProsthesis, Nose, Internal1
KGZAccessories, Catheter1
LZKImplant, Malar1
MDAElastomer, Silicone, For Scar Management1
MICImplant, Muscle, Pectoralis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 23, 2003K023678DIMISIL SCAR GEL
Aesthetic and Reconstructive Technologies, Inc.
MDA
Oct 10, 2002K022306AART SILICONE TUBING
Aesthetic and Reconstructive Technologies, Inc.
KGZ
Aug 26, 2002K022511AART CALF IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
MIB
Aug 8, 2002K022223AART SILICONE SHEETING
Aesthetic and Reconstructive Technologies, Inc.
MIB
Jul 16, 2002K021839AART GLUTEAL IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
MIB
Jul 16, 2002K021820AART SILICONE CARVING BLOCK
Aesthetic and Reconstructive Technologies, Inc.
MIB
Jul 3, 2002K021337AART PECTORALIS IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
MIC
Jul 2, 2002K021419AART MALAR IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
LZK
Jul 2, 2002K021418AART NASAL IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
FZE
Jul 2, 2002K021417AART CHIN IMPLANT
Aesthetic and Reconstructive Technologies, Inc.
FWP

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes