Skip to content

Medline MDS876630

by Medline Industries, Inc.

Medline MDS876630 is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 24 Nov 2020 (UDI-DI 10884389141595), 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 Number10884389141595 UDI-DI Date24 Nov 2020ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Oral care kit, single-use
Model / Ref / Catalog
MDS876630
Primary DI / UDI-DI
10884389141595
FDA product code
NXZ
GMDN term
Oral care kit, single-use
Device class
Class I
Regulation number
872.6855
GUDID distribution status
In Commercial Distribution

Related devices

Category: Oral care kit, single-use

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)