Skip to content

Smart Dx

by Bts SpA

Smart Dx (BTSSDX) is a Class II device made by Bts SpA, cleared under FDA 510(k) K131660 on 17 Apr 2014 and listed in FDA GUDID since 12 Feb 2017 (UDI-DI B179SDX), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K131660

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB179SDX UDI-DI Date12 Feb 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131660 Date17 Apr 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131660 decided 17 Apr 2014 Active
  • FDA GUDID UDI-DI B179SDX listed 12 Feb 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131660
  2. Listed FDA GUDID B179SDX

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Smart
Generic name
Biomechanical function analysis system, motion-tracking
Model / Ref / Catalog
DX, BTSSDX
Primary DI / UDI-DI
B179SDX
510(k) Number
FDA product code
LXJ
GMDN term
Biomechanical function analysis system, motion-tracking
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LXJ (System, Optical Position/Movement Recording).

Other devices from Bts SpA

  • Smart Dx Evo Hybrid

    Class II
  • Tmjoint 1.0

    Class II
  • Smart Dx EVO2

    Class II
  • P6000

    Class I

See all devices from Bts SpA →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)