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Companies / Nexpring Health
Medical device company profile

Nexpring Health

Global assisted reproductive technology group spanning IVF equipment, devices, consumables and media.

Manufacturer / DeveloperWomen’s & Reproductive HealthCommercial-stage
HeadquartersNot established
FoundedNot confirmed
Commercial statusCommercially availableART devices, consumables and media are marketed internationally through group businesses.
EmployeesNot confirmed
Estimated revenueNot confirmed
Official websitewww.nexpringhealth.com ↗

Company overview

Nexpring Health brings together assisted reproductive technology businesses serving fertility clinics and laboratories. Its brand portfolio includes Hamilton Thorne, Cook Reproductive Health, Planer, Gynemed, Gynétics, IVFtech and acquired Irvine Scientific ART and cytogenetics product lines.

The group combines manufacturing with distribution and technical services across the fertility workflow. Its device portfolio includes embryo-manipulation lasers, incubators and reproductive procedure instruments. The catalog also contains third-party equipment, so a listed product is not automatically manufactured by Nexpring or one of its businesses.

[1][2][3][4][12][13][14][17]

Leadership

2 people
Wil BorenChief Executive Officer [14]
Jimmy DeStephensChief Operating Officer / Chief Financial Officer [14]

Products & regulatory status How does MedTechIndex get this information?

Summary

Hamilton Thorne’s LYKOS family is documented under K120055 and K202241, the latter covering the dynamic targeting system. These records retain Hamilton Thorne as the original applicant. Legacy Cook Mini-Incubator clearance K983642 concerns the earlier incubator lineage and is not assigned to MINC+. [5][6][7]

FDA lists an open Class II recall, Z-0722-2024, for specified lots of MINC+ K-MINC-2000 / G44429 because electrostatic discharge can disrupt temperature control. Older MINC K-MINC-1000 recalls Z-1377-2018 and Z-1378-2018 share one terminated event. The separate humidification-flask recall Z-0809-2021 is also terminated. [11][8][9][10]

Regulatory snapshot How to read this snapshot

U.S. FDA
2+
510(k) clearances
0
De Novo grants
0
PMA approvals
1
Recall events

Latest recorded source review: 2026-10-30.

Scope: selected product families.

View 1 documented open recall event
Documented open FDA recall events
Recalled product / recordInitiatedSource
  • MINC+ K-MINC-2000 / G44429; affected lotsZ-0722-2024
December 7, 2023[11]

Commercial portfolio snapshot

Documented commercial product families.

LYKOS / LYKOS DTS — official manufacturer product image
Image: Hamilton Thorne / Nexpring Health
IVF laser system

LYKOS / LYKOS DTS ↗

Hamilton Thorne laser systems used for assisted hatching, zona pellucida thinning and embryo biopsy in clinical IVF workflows. [15]

FDA 510(k)-cleared LYKOS family

Marketed through the Hamilton Thorne business.

MINC+ Benchtop Incubator — official manufacturer product image
Image: Nexpring Health / Cook Reproductive Health
IVF incubator

MINC+ Benchtop Incubator ↗

Benchtop incubator with independently humidified chambers for assisted reproduction laboratory workflows. [16]

Commercially offered · specified-lot FDA recall documented

Marketed through the Cook Reproductive Health portfolio.

17 Cited Sources

Accessed 10/30/2026

Last substantive review: 10/30/2026

[1] FDA 510(k) database — research search ↗U.S. Food and Drug Administration · regulatory databaseFDA database search page; not an individual device record.
[2] FDA enforcement reports database — research search ↗U.S. Food and Drug Administration · regulatory databaseFDA database search page; not an individual device record.
[3] FDA PMA database — research search ↗U.S. Food and Drug Administration · regulatory databaseFDA database search page; not an individual device record.
[4] FDA medical-device recall database — research search ↗U.S. Food and Drug Administration · regulatory databaseFDA database search page; not an individual device record.
[5] FDA 510(k) decision K120055 ↗U.S. Food and Drug Administration · regulatory database
[6] FDA 510(k) decision K202241 ↗U.S. Food and Drug Administration · regulatory database
[7] FDA 510(k) decision K983642 ↗U.S. Food and Drug Administration · regulatory database
[8] FDA recall record 163146 ↗U.S. Food and Drug Administration · regulatory database
[9] FDA recall record 163147 ↗U.S. Food and Drug Administration · regulatory database
[10] FDA recall record 184946 ↗U.S. Food and Drug Administration · regulatory database
[11] FDA recall record 205087 ↗U.S. Food and Drug Administration · regulatory database
[12] Group and brand portfolio ↗Nexpring Health · company website
[13] Group announcements and acquisitions ↗Nexpring Health · company website
[14] Company history and executive leadership ↗Nexpring Health · company website
[15] Hamilton Thorne LYKOS / LYKOS DTS ↗Nexpring Health · company website
[16] MINC+ benchtop incubator ↗Nexpring Health · company website
[17] Manufacturing and quality ↗Nexpring Health · company website
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