Medical Device Manufacturer · US , Greenwich , CT

Li Medical Technologies, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1993

Total

Cleared

Denied

Li Medical Technologies, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in Greenwich, US.

Historical record: 17 cleared submissions from 1993 to 2000.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Li Medical Technologies, Inc.

17 devices

1-17 of 17

Cleared Sep 19, 2000

ULTRASORB SUTURE ANCHOR

K002413 · MAI

Orthopedic · 43d

Cleared Oct 27, 1999

ROTORBLADE SUTURE ANCHOR

K993373 · MAI

Orthopedic · 20d

Cleared Sep 23, 1999

ROTORBLADE SUTURE ANCHOR

LM BONE ANCHOR (ORTHOPEDICS)

K963812 · MBI

Orthopedic · 64d

Cleared Apr 30, 1996

LM ANCHOR OR OTHER PROPRIETARY NAME

LMT ARTHROSCOPIC SUTURING INSTRUMENTS

K941964 · HRX

Orthopedic · 159d

Cleared Jan 25, 1994

LAPORASCOPIC CANNULA SEAL

K933025 · GCJ

General & Plastic Surgery · 217d

Cleared Jun 25, 1993

INSTRUMENTS FOR LAPAROSCOPIC USE

K931142 · GCJ

General & Plastic Surgery · 112d

Li Medical Technologies, Inc. - FDA 510(k) Cleared Devices

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