Phx Technologies Corp. - FDA 510(k) Cleared Devices
49
Total
49
Cleared
0
Denied
Phx Technologies Corp. has 49 FDA 510(k) cleared general & plastic surgery devices. Based in Denton, US.
Historical record: 49 cleared submissions from 1993 to 1998.
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.
49 devices
Cleared
Jan 09, 1998
WINGED NEEDLE HOLDER
Gastroenterology & Urology
52d
Cleared
Jun 27, 1997
STONE EXTRACTOR
Gastroenterology & Urology
92d
Cleared
Nov 14, 1995
RETROGRADE KNIFE
Orthopedic
47d
Cleared
Nov 14, 1995
RETRACTOR
Orthopedic
47d
Cleared
Nov 14, 1995
PROBE KNIFE
Orthopedic
47d
Cleared
Nov 14, 1995
RRIANGLE KNIFE
Orthopedic
47d
Cleared
Oct 23, 1995
BOAT NOSE OBTURATOR
Orthopedic
28d
Cleared
Oct 23, 1995
CONICAL OBTURATOR
Orthopedic
28d
Cleared
Oct 23, 1995
DISSECTING OBTURATOR
Orthopedic
28d
Cleared
Oct 23, 1995
CARPAL TUNNEL SLOTTED CANNULA
Orthopedic
28d
Cleared
Oct 23, 1995
BLUNT DISSECTOR, CURVED
Orthopedic
27d
Cleared
Oct 23, 1995
PROBE
Orthopedic
27d
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