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TRUEplus 5-bevel Pen Needle 32G 4mm

by Trividia Health, Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00050428167267 UDI-DI Date7 Oct 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
TRUEplus
Generic Name
Autoinjector needle
Model / Ref / Catalog
TRUEplus 5-bevel Pen Needle 32G 4mm, S6007A32-50
Primary DI / UDI-DI
00050428167267
510(k) Number
FDA Product Code
FMI
GMDN Term
Autoinjector needle
Device Class
Class II
Regulation Number
880.5570
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 32 Gauge
Length — 0.157 Inch

From the manufacturer

Manufacturer's product page: TRUEplus® Pen Needles

Related devices

Cleared under the same submission (K180720)

Show all (12)

Other devices from Trividia Health, Inc.

See all devices from Trividia Health, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No