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Pilling IPN017937

by Teleflex Incorporated

Pilling IPN017937 (P16425) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 14026704792334), 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 Number14026704792334 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  • Withdrawn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
Orthopaedic implantable-device cutter
Model / Ref / Catalog
IPN017937, P16425
Primary DI / UDI-DI
14026704792334
FDA product code
HXZ
GMDN term
Orthopaedic implantable-device cutter
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implantable-device cutter

Similar devices in this category

Other devices filed under Orthopaedic implantable-device cutter.

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)