Rexton, Inc.
FDA 510(k) medical device clearances.
Top product codes for Rexton, Inc.
Recent clearances by Rexton, Inc.
- K970537 — REXTON MODEL 48 AND 49PP
- K964451 — PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATC
- K960295 — LONG LIFE RX-12
- K954922 — REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE INSTRUMENTS
- K953770 — REXTON MINI-PRIMO PLUS, PP142, D.C .H.I. FAMILY
- K950451 — M-29 PP-PC, M-29 PP-O/PC
- K944851 — MICRO MINI PRIMO AGC, MICRO-MINI PRIMO S-AGC
- K944777 — ORION PPM, PP, PP-D
- K944359 — EXPRESSION RX-12, ENHANCEMENT RX-34, ELITE RX-12
- K942702 — DEEP CANAL HEARING INSTRUMENT
- K944548 — REXPLUS PP3
- K915683 — REXTON RX12 WITH HORIZON PROGRAMMABLE OPTION
- K915684 — REXTON RX34 WITH HORIZON PROGRAMMABLE OPTION
- K901341 — REXTON RX12 POWER PLUS W/DUAL RECEIVER
- K900636 — REXTON PP 142, PP 142-L
- K896057 — MINI PRIMO PLUS ASP BEHIND-THE-EAR HEARING AID
- K896056 — REXTON RX12D CUSTOM IN-THE-EAR HEARING AID
- K892898 — ASTRO BEHIND-THE-EAR HEARING AID
- K892333 — REXTON RX12PP, RX20PP & RX34PP IN-THE-EAR HEAR AID
- K861532 — RX-33S INTRA MINI CANAL MODULE
- K832180 — REXTON RX10, RX20-30 & 40
Data sourced from openFDA. This site is unofficial and independent of the FDA.