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Bio Protech MaxTens 1k Unit

by Bio Protech USA, Inc.

Bio Protech MaxTens 1k Unit is a medical device (FDA Class II; FDA product code GZJ, Stimulator, Nerve, Transcutaneous, For Pain Relief) made by Bio Protech USA, Inc., cleared under FDA 510(k) K073438 on 7 Feb 2008 and listed in FDA GUDID since 1 Sep 2016 (UDI-DI 00817120020562), active as of 22 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 22 Oct 2026

Documents

510(k) K073438

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817120020562 UDI-DI Date1 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK073438 Date7 Feb 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K073438 decided 7 Feb 2008 Active
  • FDA GUDID UDI-DI 00817120020562 listed 1 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K073438
  2. Listed FDA GUDID 00817120020562

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Bio Protech
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / reference
MaxTens 1k Unit
Primary DI / UDI-DI
00817120020562
510(k) Number
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

Cleared under the same submission (K073438)

and 4 more cleared under K073438

Similar devices

Other devices filed under FDA product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief).

Other devices from Bio Protech USA, Inc.

See all devices from Bio Protech USA, Inc. →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)