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Dekalb Knee Pack DM210

by Packroom LLC

Dekalb Knee Pack DM210 is a device made by Packroom LLC, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 00817395020090), 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 Number00817395020090 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Dekalb Knee Pack
Generic name
Joint prosthesis implantation kit, single-use
Model / reference
DM210
Primary DI / UDI-DI
00817395020090
GMDN term
Joint prosthesis implantation kit, single-use
GUDID distribution status
In Commercial Distribution

Related devices

Category: Joint prosthesis implantation kit, single-use

Similar devices in this category

Other devices filed under Joint prosthesis implantation kit, single-use.

Other devices from Packroom LLC

See all devices from Packroom LLC →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Lot / batch number
Other properties (11, all answered No)