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STABLYX, CMC Implant, Sz. 1

by Skeletal Dynamics L.L.C. 2 variants

STABLYX, CMC Implant, Sz. 1 (STX-IS1) is a Class II device made by Skeletal Dynamics L.L.C., listed in FDA GUDID since 21 Oct 2016 (UDI-DI 00841506104348), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841506104348 UDI-DI Date21 Oct 2016ListedStatusListed 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  • Withdrawn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
Stablyx
Generic name
Metacarpal prosthesis
Model / Ref / Catalog
STABLYX, CMC Implant, Sz. 1, STX-IS1
Primary DI / UDI-DI
00841506104348
FDA product code
KYI
GMDN term
Metacarpal prosthesis
Device class
Class II
Regulation number
888.3770
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KYI (PROSTHESIS, WRIST, CARPAL TRAPEZIUM).

Other devices from Skeletal Dynamics L.L.C.

See all devices from Skeletal Dynamics L.L.C. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)