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DynaNail 1200-06-1022

by Medshape, Inc.

DynaNail 1200-06-1022 is a Class II device made by Medshape, Inc., listed in FDA GUDID since 16 Oct 2025 (UDI-DI M97012000610220), 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 NumberM97012000610220 UDI-DI Date16 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
DynaNail
Generic name
Arthrodesis intramedullary nail, non-distracting
Model / reference
1200-06-1022
Primary DI / UDI-DI
M97012000610220
FDA product code
HSB
GMDN term
Arthrodesis intramedullary nail, non-distracting
Device class
Class II
Regulation number
888.3020
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Similar devices

Other devices filed under FDA product code HSB (Rod, Fixation, Intramedullary And Accessories).

Other devices from Medshape, Inc.

See all devices from Medshape, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)