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FLYp 0002

by Convexity Scientific, LLC

FLYp 0002 is an ultrasonic nebulizing system (FDA Class II; FDA product code CAF, Nebulizer (Direct Patient Interface)) made by Convexity Scientific, LLC, listed in FDA GUDID since 8 Apr 2021 (UDI-DI 00869112000168), 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 Number00869112000168 UDI-DI Date8 Apr 2021ListedStatusListed 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  • Withdrawn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
FLYp
Generic name
Ultrasonic nebulizing system
Model / reference
0002
Primary DI / UDI-DI
00869112000168
FDA product code
CAF
GMDN term
Ultrasonic nebulizing system
Device class
Class II
Regulation number
868.5630
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic nebulizing system

Similar devices

Other devices filed under FDA product code CAF (Nebulizer (Direct Patient Interface)).

Other devices from Convexity Scientific, LLC

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)