# Embryotech Laboratories, Inc.

- Location (FDA's records): Wayland, MA
- FDA decisions: 2 (1998–2001): 2 510(k) clearances
- Product codes: POV (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Humagen Fertility Diagnostics, Inc.: 1 (https://510kreport.com/company/humagen-fertility-diagnostics)

## Firms that cite its devices most
- Princeton BioMeditech Corp.: 2 (https://510kreport.com/company/princeton-biomeditech)
- Genosis, Ltd.: 1 (https://510kreport.com/company/genosis)

## Its most-cited devices
- K011679: Fertilmarq Home Diagnostic Screening Test Kit for Male Infertility (2001), cited by 3
- K983473: Fertilmarq Test Kit (1998), cited by 1

## Recent decisions
- K011679: Fertilmarq Home Diagnostic Screening Test Kit for Male Infertility (Aug 15, 2001)
- K983473: Fertilmarq Test Kit (Dec 17, 1998)

Source page: https://510kreport.com/company/embryotech-laboratories