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Numi NU70001

by Quest USA Corp.

Numi NU70001 is a Class I device made by Quest USA Corp., listed in FDA GUDID since 1 Aug 2024 (UDI-DI 00810146467182), 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 Number00810146467182 UDI-DI Date1 Aug 2024ListedStatusListed 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  • Withdrawn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
Numi
Generic name
Teething device, non-fluid-filled
Model / reference
NU70001
Primary DI / UDI-DI
00810146467182
FDA product code
MEF
GMDN term
Teething device, non-fluid-filled
Device class
Class I
Regulation number
872.5550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Teething device, non-fluid-filled

Other devices from Quest USA Corp.

See all devices from Quest USA Corp. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)