Skip to content

ELEOS™ Limb Salvage System with NanoCept® Technology AM-MS-070MM-C

by Onkos Surgical, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 NumberB278AMMS070MMC0 UDI-DI Date28 Aug 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ELEOS™ Limb Salvage System with NanoCept® Technology
Generic Name
Body femoral/tibial extension stem, coated
Model / Ref / Catalog
AM-MS-070MM-C
Primary DI / UDI-DI
B278AMMS070MMC0
De Novo Number
FDA Product Code
QZZ
GMDN Term
Body femoral/tibial extension stem, coated
Device Class
Class II
Regulation Number
888.3900
GUDID distribution status
In Commercial Distribution
Size
Length — 70 Millimeter

Related devices

Cleared under the same submission (DEN210058)

Other devices from Onkos Surgical, Inc.

See all devices from Onkos Surgical, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No