Product code LDK— Unknown

CONTOUROGRAPH M-500

Classification name: Device, Sensing, Optical Contour
Device class: Unclassified
Advisory panel: Unknown
Total cleared: 8
First cleared: 1980-04-02
Most recent: 2023-11-15

Market context for product code LDK

FDA has cleared 8 devices under product code LDK between 1980 and 2023, filed by 8 applicant companies. No FDA device recalls reference this product code.

Clearances per year

20232 clearances
20191 clearance
19941 clearance
19861 clearance
19852 clearances
19801 clearance

Top applicants under product code LDK

Terran Biomedical Instruments1 clearance
Quantec Image Processing , Ltd.1 clearance
Oxford Medilog, Inc.1 clearance
Nsite, Inc.1 clearance
Momentum Health, Inc.1 clearance
Far Orthopedics, Inc.1 clearance
Cryos Technologies, Inc.1 clearance
Bio-Tek Instruments, Inc.1 clearance

Recent clearances under product code LDK

K230463 — NSite Scoliosis Assessment AppNsite, Inc.·2023-11-15
K232023 — Momentum SpineMomentum Health, Inc.·2023-10-04
K183485 — CryoVizion SystemCryos Technologies, Inc.·2019-08-28
K923792 — QUANTEC SPINAL MEASUEMENT SYSTEMQuantec Image Processing , Ltd.·1994-04-20
K860225 — METRICOMFar Orthopedics, Inc.·1986-02-11
K851133 — TERRAN BIOMECHANICAL ANALYSIS SYSTEMTerran Biomedical Instruments·1985-06-19
K844736 — ISISOxford Medilog, Inc.·1985-03-21
K800591 — CONTOUROGRAPH M-500Bio-Tek Instruments, Inc.·1980-04-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.