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Henry Schein 5702069

by Henry Schein, Inc.

Henry Schein 5702069 is a Class II device made by Henry Schein, Inc., cleared under FDA 510(k) K172763 on 4 Jun 2018 and listed in FDA GUDID since 7 Jan 2021 (UDI-DI 10304040132385), 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) K172763

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 Number10304040132385 UDI-DI Date7 Jan 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK172763 Date4 Jun 2018IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K172763 decided 4 Jun 2018 Active
  • FDA GUDID UDI-DI 10304040132385 listed 7 Jan 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K172763
  2. Listed FDA GUDID 10304040132385

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Henry Schein
Generic name
Blood collection tube holder/needle
Model / Ref / Catalog
5702069
Primary DI / UDI-DI
10304040132385
510(k) Number
FDA product code
FMI
GMDN term
Blood collection tube holder/needle
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FMI (Needle, hypodermic, single lumen).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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