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Pilling IPN019443

by Teleflex Incorporated

Pilling IPN019443 (P21559) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 14026704797315), 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 Number14026704797315 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Pilling
Generic name
General-purpose curette
Model / Ref / Catalog
IPN019443, P21559
Primary DI / UDI-DI
14026704797315
FDA product code
GZX
GMDN term
General-purpose curette
Device class
Class I
Regulation number
882.4525
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General-purpose curette

Other devices from Teleflex Incorporated

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    Class II

See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)