Rexton, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rexton, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Rexton, Inc. has 21 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1983 to 1997.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rexton, Inc.
21 devices
Cleared
Mar 28, 1997
REXTON MODEL 48 AND 49PP
Ear, Nose, Throat
44d
Cleared
Nov 27, 1996
PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATC
Ear, Nose, Throat
21d
Cleared
Mar 22, 1996
LONG LIFE RX-12
Ear, Nose, Throat
60d
Cleared
Jan 17, 1996
REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE...
Ear, Nose, Throat
83d
Cleared
Sep 18, 1995
REXTON MINI-PRIMO PLUS, PP142, D.C .H.I. FAMILY
Ear, Nose, Throat
35d
Cleared
Mar 21, 1995
M-29 PP-PC, M-29 PP-O/PC
Ear, Nose, Throat
46d
Cleared
Feb 22, 1995
MICRO MINI PRIMO AGC, MICRO-MINI PRIMO S-AGC
Ear, Nose, Throat
145d
Cleared
Dec 30, 1994
ORION PPM, PP, PP-D
Ear, Nose, Throat
94d
Cleared
Dec 29, 1994
EXPRESSION RX-12, ENHANCEMENT RX-34, ELITE RX-12
Ear, Nose, Throat
113d
Cleared
Dec 21, 1994
DEEP CANAL HEARING INSTRUMENT
Ear, Nose, Throat
196d
Cleared
Nov 14, 1994
REXPLUS PP3
Ear, Nose, Throat
59d
Cleared
Jan 09, 1992
REXTON RX12 WITH HORIZON PROGRAMMABLE OPTION
Ear, Nose, Throat
21d