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McDavid MD31350-50090-L

by Shock Doctor, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00029369185388 UDI-DI Date1 Sep 2026ListedStatusListed 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  • Withdrawn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
McDavid
Generic Name
Orthotic insole, prefabricated, non-antimicrobial
Model / Reference
MD31350-50090-L
Primary DI / UDI-DI
00029369185388
FDA Product Code
KYS
GMDN Term
Orthotic insole, prefabricated, non-antimicrobial
Device Class
Class I
Regulation Number
880.6280
GUDID distribution status
In Commercial Distribution

Other devices from Shock Doctor, Inc.

See all devices from Shock Doctor, Inc. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No