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BodyMed ZZAN602

by Boxout, LLC

BodyMed ZZAN602 is a Class II device made by Boxout, LLC, listed in FDA GUDID since 5 Sep 2016 (UDI-DI 00815802014496), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00815802014496 UDI-DI Date5 Sep 2016ListedStatusListed 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  • Withdrawn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
BodyMed
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / Ref / Catalog
ZZAN602
Primary DI / UDI-DI
00815802014496
FDA product code
GZJ
GMDN term
Physical therapy transcutaneous neuromuscular electrical stimulation system
Device class
Class II
Regulation number
882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

Similar devices in this category

Other devices filed under Physical therapy transcutaneous neuromuscular electrical stimulation system.

Other devices from Boxout, LLC

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)