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STABLYX, Metacarpal Rasp, Sz. 3

by Skeletal Dynamics L.L.C. 3 variants

STABLYX, Metacarpal Rasp, Sz. 3 (STX-CMA-MR3) is a Class II device made by Skeletal Dynamics L.L.C., listed in FDA GUDID since 30 Oct 2015 (UDI-DI 00841506103143), 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 Number00841506103143 UDI-DI Date30 Oct 2015ListedStatusListed 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  • Withdrawn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, Metacarpal Rasp, Sz. 3, STX-CMA-MR3
Primary DI / UDI-DI
00841506103143
FDA product code
HSB
GMDN term
Metacarpal prosthesis
Device class
Class II
Regulation number
888.3020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Metacarpal prosthesis

Similar devices

Other devices filed under FDA product code HSB (ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES).

Other devices from Skeletal Dynamics L.L.C.

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

Properties

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