Meet INVOCELL

An innovative option used in fertility treatment that considers your concerns about cost

INVOCELL was designed to offer you a different
option and hope on your fertility journey.

INVOCELL is an intravaginal culture (IVC) system
and consists of the INVOCELL culture
and retention
devices. The first and only FDA-cleared option
of its kind used in fertility treatment, INVOCELL
uses your
body as an incubator for fertilization, making you an
even greater part of the process.

In a clinical trial, about
1 in 4 embryo
transfers
resulted in a birth

An innovative option that
considers your
concerns
about treatment costs

Unique method
that uses
your
own body as
an incubator

Used with
mild ovarian
stimulation

May require
fewer monitoring
visits,
as decided by
your doctor

FIND OUT WHAT INVOCELL
COULD MEAN FOR YOU

Get to know INVOCELL

A first-of-its-kind device used in fertility treatment,
INVOCELL holds the eggs and sperm in your body for
fertilization and incubation, allowing you to be more
personally involved in the process.

WHAT TO EXPECT WITH INVOCELL

Find a fertility specialist who offers INVOCELL

As you navigate your fertility journey, finding a doctor—one who specializes in helping people conceive—is an important step. This kind of specialist, called a reproductive endocrinologist or RE, can help you decide if INVOCELL is the right choice for you.

You can ask your fertility
specialist if she or he offers
INVOCELL, or find a fertility
center near you that does.

INDICATIONS FOR USE

INVOCELL® Intravaginal Culture System contains the INVOCELL Culture Device and INVOCELL Retention Device. The Culture Device is indicated for use in preparing, holding, and transferring human gametes or embryos during In Vitro Fertilization/Intravaginal Culture (IVF/IVC) and Intra-cytoplasmic Sperm Injection Fertilization/Intravaginal Culture (ICSI/IVC). The Retention Device is used during the incubation period to aid in holding the Culture Device in the vagina. The Culture and Retention Devices are not indicated for periods of use exceeding 72 hours.

SELECT IMPORTANT SAFETY INFORMATION

  • Do not use the Culture or Retention devices if you are unable to tolerate having a device placed within your vagina.
  • Do not use the Culture Device if you are sensitive to medical grade silicone or polystyrene or if you have a severe case of vaginitis or a history of toxic shock syndrome. Tell your doctor if you have had any recent pelvic surgery.
  • Avoid any activity such as sexual intercourse, strenuous physical activity, swimming, bathing in a tub (a shower is permissible), use of a douche, sauna, or any other activity that may alter the temperature of the vaginal cavity and avoid handling or removing the Culture and Retention Devices while in place.
  • Your doctor should explain to you what to do if the Culture and Retention Device should shift in the vagina or fall out. Call your doctor right away should this occur.

Your doctor will determine if this product is right for you and will provide you with more detailed information about the risks and benefits associated with using this device. Always follow your doctor’s instructions. Contact your doctor immediately if you have any questions or concerns before, during, or after treatment.

For more information, please see the INVOCELL Patient Information.

INDICATIONS FOR USE

INVOCELL® Intravaginal Culture System contains the INVOCELL
Culture Device and INVOCELL Retention Device. The Culture Device is
indicated
for use in preparing, holding, and transferring human
gametes or embryos during In Vitro Fertilization/Intravaginal Culture
(IVF/IVC) and
Intra-cytoplasmic Sperm Injection
Fertilization/Intravaginal Culture (ICSI/IVC). The Retention Device is
used during the incubation period to aid
in holding the Culture Device in
the vagina. The Culture and Retention Devices are not indicated for
periods of use exceeding 72 hours.

SELECT IMPORTANT SAFETY INFORMATION

  • Do not use the Culture or Retention devices if you are unable to tolerate having a device placed within your vagina.
Please see Indication and Select Important Safety Information