Medical Device Manufacturer · US , Malvern , PA

Landos, Inc. - FDA 510(k) Cleared Devices

15 submissions · 12 cleared · Since 1994

Total

Cleared

Denied

Landos, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Malvern, US.

Historical record: 12 cleared submissions from 1994 to 1997.

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 - Landos, Inc.

15 devices

1-15 of 15

Cleared Aug 05, 1997

MEMORY STAPLE (20 SIZES AVAILABLE)

K964226 · JDR

Orthopedic · 286d

Cleared Jul 09, 1997

34MM SCARF THREAD-HEAD(TM) SCREW

SCARF THREAD-HEAD (TM) HEAD SCREW

22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD

SCARF THREAD-HEAD SCREW

BIOSTOP G BONE CEMENT RESTRICTOR

K943727 · LZN

Orthopedic · 282d

Cleared Sep 12, 1994

TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS

K933108 · LZO

Orthopedic · 444d

Cleared Jun 16, 1994

MORPHOMETRIC TOTAL HIP PROSTHESIS

K935185 · LZO

Orthopedic · 233d

Cleared Jun 15, 1994

TITAN DYSPLASIC TOTAL HIP PROSTHESIS

K932935 · LZO

Orthopedic · 364d

Cleared May 16, 1994

EUROFORM TOTAL HIP PROSTHESIS

K933567 · LZO

Orthopedic · 298d

Landos, Inc. - FDA 510(k) Cleared Devices

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