Atlas FDA

LDK

8 FDA 510(k) clearances · Product code

106 daysmedian time to decision
631 days90th percentile
8clearances measured

FDA profile

Official device name
Device, Sensing, Optical Contour
Device class
Unclassified
Medical specialty
Unknown
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RecordFirmDate
NSite Scoliosis Assessment App (K230463)Nsite, Inc.2023-11-15
Momentum Spine (K232023)Momentum Health, Inc.2023-10-04
CryoVizion System (K183485)Cryos Technologies, Inc.2019-08-28
QUANTEC SPINAL MEASUEMENT SYSTEM (K923792)Quantec Image Processing , Ltd.1994-04-20
METRICOM (K860225)Far Orthopedics, Inc.1986-02-11
TERRAN BIOMECHANICAL ANALYSIS SYSTEM (K851133)Terran Biomedical Instruments1985-06-19
ISIS (K844736)Oxford Medilog, Inc.1985-03-21
CONTOUROGRAPH M-500 (K800591)Bio-Tek Instruments, Inc.1980-04-02

Track LDK automatically

Every clearance here is in the API, with alerts when new ones post.