510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851133Substantially Equivalent

Terran Biomechanical Analysis System

Terran Biomedical Instruments, Salem OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851133 is the FDA 510(k) clearance record for TERRAN BIOMECHANICAL ANALYSIS SYSTEM, cleared for Terran Biomedical Instruments on under FDA product code LDK (Device, Sensing, Optical Contour). FDA records list one 510(k) clearance for Terran Biomedical Instruments. As of , FDA records show no recalls naming K851133.

Clearance record

Decision date
Received
(90 days to decision)
Product code
LDK Device, Sensing, Optical Contour
Device class
Unclassified
Review panel
Unknown
Applicant
Terran Biomedical Instruments 1520 24th. St. NE, Salem OR
Third party review
No

Clearances, product code LDK

Trailing 12 months

FDA records hold no clearances under product code LDK in the trailing twelve months.

FDA records show no clearances under product code LDK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260