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Teleflex IPN931133

by Teleflex Incorporated

Teleflex IPN931133 (ST19) is a Class II device made by Teleflex Incorporated, cleared under FDA 510(k) K200517 on 9 Apr 2020 and listed in FDA GUDID since 3 Aug 2026 (UDI-DI 04026704934812), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K200517

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04026704934812 UDI-DI Date3 Aug 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK200517 Date9 Apr 2020IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K200517 decided 9 Apr 2020 Active
  • FDA GUDID UDI-DI 04026704934812 listed 3 Aug 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K200517
  2. Listed FDA GUDID 04026704934812

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Teleflex
Generic name
Laparoscopic trocar blade, single-use
Model / Ref / Catalog
IPN931133, ST19
Primary DI / UDI-DI
04026704934812
510(k) Number
FDA product code
GCJ
GMDN term
Laparoscopic trocar blade, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K200517)

Similar devices

Other devices filed under FDA product code GCJ (Laparoscope, general & plastic surgery).

Other devices from Teleflex Incorporated

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See all devices from Teleflex Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)