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NeckCare Home v1

by NeckCare Holding ehf

NeckCare Home v1 is a Class II device made by NeckCare Holding ehf, listed in FDA GUDID since 9 Mar 2026 (UDI-DI 05694230564040), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05694230564040 UDI-DI Date9 Mar 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
NeckCare Home
Generic name
Biomechanical function analysis/rehabilitation software
Model / reference
v1
Primary DI / UDI-DI
05694230564040
FDA product code
QKC
GMDN term
Biomechanical function analysis/rehabilitation software
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Other devices from NeckCare Holding ehf

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)