Implantech Associates, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Implantech Associates, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Customized Contour Implant, Customized Contour Implant, ePTFE-Coated Auricular Implant
41
Total
40
Cleared
0
Denied
Implantech Associates, Inc. has 40 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, US.
Historical record: 40 cleared submissions from 1989 to 2020.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Acknowledge Regulatory Strategies, LLC and Acknowledge Regulatory Strategies.
FDA 510(k) Regulatory Record - Implantech Associates, Inc.
41 devices
Cleared
Dec 23, 2020
Customized Contour Implant
General & Plastic Surgery
289d
Cleared
Aug 23, 2019
Customized Contour Implant
General & Plastic Surgery
116d
Cleared
Jul 18, 2018
ePTFE-Coated Auricular Implant
General & Plastic Surgery
344d
Cleared
Jul 10, 2014
3D EPTFE
General & Plastic Surgery
79d
Cleared
Aug 31, 2007
IMPLANTECH EPTFE SHEETING, MODEL EPTFE-XXX
General & Plastic Surgery
94d
Cleared
Nov 04, 2005
GLUTEAL IMPLANT, MODELS RND 5-X, TRD 6-X
General & Plastic Surgery
52d
Cleared
Nov 04, 2005
CALF IMPLANT, MODEL EC17-X
General & Plastic Surgery
52d
Cleared
Feb 07, 2002
GELZONE
General & Plastic Surgery
90d
Cleared
Oct 24, 2001
CONFORM SHEETING, MODEL IGEL
General & Plastic Surgery
86d
Cleared
Nov 24, 2000
IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL)
General & Plastic Surgery
70d
Cleared
Nov 07, 1997
IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT
General & Plastic Surgery
52d
Cleared
Feb 12, 1997
IMPLATECH RP MEDICAL GRADE SILICONE GEL SHEETING
General & Plastic Surgery
71d
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