Medical Device Manufacturer · US , E Providence , RI

Lima Intl. Corp. - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 1989

8

Total

7

Cleared

0

Denied

Lima Intl. Corp. has 7 FDA 510(k) cleared medical devices. Based in E Providence, US.

Historical record: 7 cleared submissions from 1989 to 1994. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Lima Intl. Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lima Intl. Corp.

8 devices

1-8 of 8

Cleared Apr 05, 1994

CL HIP STEM H/A COATED

Orthopedic · 672d

Cleared Jun 14, 1991

LIMA COLLARED CL STEM

Orthopedic · 107d

Cleared Jan 01, 1991

PGR HIP STEM (ENDOPROSTHESIS) FOR LARGE BONE RESEC

Orthopedic · 392d

Cleared Oct 03, 1990

MOORE TYPE ENDO PROSTHESIS

Orthopedic · 273d

Cleared Sep 11, 1990

SL-SELF LOCKING TOTAL HIP-FEMORAL COMPONENT

Orthopedic · 89d

Cleared Jun 05, 1990

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE

Orthopedic · 182d

Cleared Apr 18, 1990

MULLER TYPE ACETABULAR CUP

Orthopedic · 91d

Cleared Apr 24, 1989

CL UNIVERSAL HIP DEVICE

Orthopedic · 130d