Microline Pentax, Inc. is one of 20410 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microline Pentax, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL M/L-10, ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS, DISPOSABLE RE-NEW FORCEPS
12
Total
12
Cleared
0
Denied
Microline Pentax, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Devers, US.
Historical record: 12 cleared submissions from 1988 to 2002.
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.
FDA 510(k) Regulatory Record - Microline Pentax, Inc.
12 devices
Cleared
Jan 08, 2002
MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM...
General & Plastic Surgery
62d
Cleared
Oct 21, 1998
ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS
General & Plastic Surgery
56d
Cleared
May 29, 1998
DISPOSABLE RE-NEW FORCEPS
General & Plastic Surgery
43d
Cleared
May 20, 1998
ELECTROSURGICAL CAUTERY PROBES
General & Plastic Surgery
48d
Cleared
Mar 27, 1998
3 MM SELEC-TIP LAPAROSCOPIC SCISSORS
General & Plastic Surgery
28d
Cleared
Jan 22, 1998
RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS
General & Plastic Surgery
87d
Cleared
Mar 28, 1997
SELECTA-TIP LAPAROSCOPIC SCISSORS
General & Plastic Surgery
22d
Cleared
Aug 09, 1996
RE-NEW LAPAROSCOPIC INSTRUMENTS
General & Plastic Surgery
70d
Cleared
Oct 12, 1993
QUICK SWITCH LAPAROSCOPIC INSTRUMENTS
General & Plastic Surgery
132d
Cleared
Apr 04, 1990
INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.
Ophthalmic
105d
Cleared
Sep 12, 1988
BRADBURY INTRAOCULAR RETINAL KIT CAT #200
Ophthalmic
185d
Cleared
May 26, 1988
MICROLINE CAT #100
Ophthalmic
80d