Ranfac, Corp. is one of 4736 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ranfac, Corp. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Ranfac, Corp. has 12 FDA 510(k) cleared medical devices. Based in Avon, US.
Historical record: 12 cleared submissions from 1985 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ranfac, Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ranfac, Corp.
12 devices
Cleared
Jan 19, 2017
Ranfac Fat Aspiration Cannula
General & Plastic Surgery
91d
Cleared
Oct 19, 2015
Ranfac Fat Aspiration Transfer Syringe (FATS) Procedure Pack, Ranfac Fat...
General & Plastic Surgery
269d
Cleared
May 22, 2015
Marrow Cellution Bone Marrow Aspiration Needle
Gastroenterology & Urology
77d
Cleared
Sep 11, 2014
RANFAC ASPIRATION NEEDLE WITH ADJUSTABLE GUIDE
Gastroenterology & Urology
147d
Cleared
Oct 22, 2013
RANFAC BONE MARROW ASPIRATION NEEDLE
Gastroenterology & Urology
181d
Cleared
May 23, 2003
RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLE
Gastroenterology & Urology
24d
Cleared
Aug 22, 2001
SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW
Gastroenterology & Urology
67d
Cleared
Aug 09, 1996
RDP-2
Obstetrics & Gynecology
84d
Cleared
Jul 11, 1995
INTRODUCER
General & Plastic Surgery
124d
Cleared
Jul 23, 1993
NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
Gastroenterology & Urology
176d
Cleared
Nov 05, 1986
RANFAC CUT BIOPSY NEEDLE
General & Plastic Surgery
14d
Cleared
Mar 11, 1985
BREAST & FOREIGN BODY LOCALIZATION INSTRUMENT
General & Plastic Surgery
74d