Are you FDA certified?

Updated 3 weeks ago by Erika

Yes, the Keto-Mojo TD-4279 meter is an FDA-approved class II medical device for the in vitro self-testing of glucose and ketone levels, and it's suitable for testing for Type 1, Type 2, and gestational diabetes.

The meter is manufactured in an FDA-inspected and -approved establishment that also conforms to  ISO:9001 manufacturing practices. The meter also conforms to ISO 15197:2013 standards. 

Here are more specifics, in case you're interested:

  • Keto-Mojo TD-4279 FDA device listing number:D126843
  • Keto-Check, Inc FDA registration number: 10055466
  • Manufacturing facility FDA establishment registration number 3004145393
  • All our inventory is stored in an FDA-registered warehouse in Los Angeles. Registration number 12631797414
  • Complete supply-chain custody is maintained throughout to assure you of genuine, quality products 


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