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At Lady Technologies Inc., we strive to deliver safe and effective products that meet all applicable regulatory requirements.

Please note that kegg is not FDA-approved for use as a contraceptive. kegg is intended to be a fertility monitor.

We have determined that kegg is a Class 1 510(k) exempt product per the NGE product code requirements and requires appropriate GMP implementation and FDA establishment registration and listing. The company is implementing the GMP system and will FDA registered and listed at shipping as required.

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