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Xpansion® Micro-Autografting Kit NHMS

by New Horizon Healthcare Management LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850084501012 UDI-DI Date28 Jul 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  • Withdrawn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
Xpansion® Micro-Autografting Kit
Generic Name
Dermatome blade, single-use
Model / Reference
NHMS
Primary DI / UDI-DI
00850084501012
FDA Product Code
GDF
GMDN Term
Dermatome blade, single-use
Device Class
Class I
Regulation Number
878.4800
GUDID distribution status
In Commercial Distribution

Other devices from New Horizon Healthcare Management LLC

See all devices from New Horizon Healthcare Management LLC →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No