Who is the manufacturer of ARTSMedia In Vitro Culture Medium (AM-IVC Medium)?

Artsmedia Denmark Aps filed the 510(k) submission for ARTSMedia In Vitro Culture Medium (AM-IVC Medium) (K220715).

What is the FDA product code for ARTSMedia In Vitro Culture Medium (AM-IVC Medium)?

MQL. It is classified under 21 CFR 884.6180 as a Class 2 device in the Obstetrics/Gynecology panel.

What is the regulatory pathway for ARTSMedia In Vitro Culture Medium (AM-IVC Medium)?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like ARTSMedia In Vitro Culture Medium (AM-IVC Medium)?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

ARTSMedia In Vitro Culture Medium (AM-IVC Medium)

K220715 · Artsmedia Denmark Aps · MQL · Feb 10, 2023 · Obstetrics/Gynecology

Device Facts

Record ID	K220715
Device Name	ARTSMedia In Vitro Culture Medium (AM-IVC Medium)
Applicant	Artsmedia Denmark Aps
Product Code	MQL · Obstetrics/Gynecology
Decision Date	Feb 10, 2023
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 884.6180
Device Class	Class 2

Intended Use

ARTSMedia In Vitro Culture Medium (AM-IVC Medium) is a culture medium intended for in vitro fertilization and in vitro culture of human gametes and embryos from fertilization until the blastocyst stage of development (day 5). The medium can also be used for embryo transfer.

Device Story

AM-IVC Medium is a sterile, single-use culture medium for human gametes and embryos; used in clinical embryology laboratories for fertilization, culture to blastocyst stage, and embryo transfer. The medium is provided in 10 mL glass bottles with Fluorotec-coated stoppers. It functions as a nutrient-rich environment supporting embryo development. Healthcare providers (embryologists/clinicians) use the medium to maintain optimal physiological conditions (pH, osmolality) for gametes and embryos outside the body. The device benefits patients by providing a controlled environment for successful fertilization and embryo development prior to transfer.

Clinical Evidence

No clinical data. Substantial equivalence supported by bench testing: biocompatibility (cytotoxicity, sensitization, vaginal irritation per ISO 10993), aseptic processing validation, shelf-life stability (real-time aging to 10 months), transportation testing (ASTM D4169-22), and 1-cell Mouse Embryo Assay (MEA) showing ≥80% development to expanded blastocysts at 96 hours.

Technological Characteristics

Formulation includes physiological salts, amino acids, vitamins, calcium lactate, EDTA, gentamicin sulphate, glucose, L-glutamine, human serum albumin, sodium bicarbonate, sodium hyaluronate, sodium pyruvate, phenol red, selenite, ethanolamine, sodium citrate, and human insulin. Sterilized via aseptic filtration. pH 7.2-7.45; osmolality 257-275 mOsm/kg; endotoxin <0.05 EU/mL. Packaging: 10 mL glass bottles with Fluorotec-coated stoppers and aluminum caps. Shelf-life: 10 months at 2-8°C.

Indications for Use

Indicated for in vitro fertilization and culture of human gametes and embryos from fertilization through the blastocyst stage (day 5) and for embryo transfer procedures.

Regulatory Classification

Identification

Reproductive media and supplement are products that are used for assisted reproduction procedures. Media include liquid and powder versions of various substances that come in direct physical contact with human gametes or embryos (including water, acid solutions used to treat gametes or embryos, rinsing solutions, sperm separation media, supplements, or oil used to cover the media) for the purposes of preparation, maintenance, transfer or storage. Supplements are specific reagents added to media to enhance specific properties of the media (e.g., proteins, sera, antibiotics, etc.).

Special Controls

*Classification.* Class II (special controls) (mouse embryo assay information, endotoxin testing, sterilization validation, design specifications, labeling requirements, biocompatibility testing, and clinical testing). The device, when it is phosphate-buffered saline used for washing, and short-term handling and manipulation of gametes and embryos; culture oil used as an overlay for culture media containing gametes and embryos; and water for assisted reproduction applications, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 884.9.

Predicate Devices

SAGE 1-Step (K133707)

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K153290 — Sydney IVF Follicle Flush Buffer, Sydney IVF Fertilization Medium, Sydney IVF Cleavage Medium, Sydney IVF Blastocyst Medium · William A. Cook Australia Pty. , Ltd. · Jan 27, 2016
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Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo for the U.S. Food & Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, with the letters "FDA" in a blue square. To the right of the square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. February 10, 2023 ARTSMedia Denmark ApS Lotte Stroebech CEO Kongevejen 149 Virum. 2830 Denmark Re: K220715 > Trade/Device Name: ARTSMedia In Vitro Culture Medium (AM-IVC Medium) Regulation Number: 21 CFR§ 884.6180 Regulation Name: Reproductive Media and Supplements Regulatory Class: II Product Code: MQL Dated: January 9, 2023 Received: January 11, 2023 Dear Lotte Stroebech: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. {1}------------------------------------------------ You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatoryinformation/postmarketing-safety-reporting-combination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, # Monica D. Garcia -S Monica D. Garcia, Ph.D. Assistant Director DHT3B: Division of Reproductive, Gynecology and Urology Devices OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration ## Indications for Use 510(k) Number (if known) K220715 Device Name ARTSMedia In Vitro Culture Medium (AM-IVC Medium) #### Indications for Use (Describe) ARTSMedia In Vitro Culture Medium) is a culture medium intended for in vitro fertilization and in vitro culture of human gametes and embryos from fertilization until the blastocyst stage of development (day 5). The medium can also be used for embryo transfer. | Type of Use (Select one or both, as applicable) | <div style="display:inline-block; vertical-align:middle; width:15px; height:15px; border: 1px solid black;"> <div style="text-align: center;">X</div> </div> Prescription Use (Part 21 CFR 801 Subpart D) <div style="display:inline-block; vertical-align:middle; width:15px; height:15px; border: 1px solid black;"></div> Over-The-Counter Use (21 CFR 801 Subpart C) | |-------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| |-------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. ***DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*** The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff [PRAStaff@fda.hhs.gov](mailto:PRAStaff@fda.hhs.gov) *"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."* ============================================================================================================================================================================== {3}------------------------------------------------ ## 510(k) Summary K220715 510(k) Owner ARTSMedia Denmark ApS Kongevejen 149 2830 Virum Denmark Lotte Stroebech Phone: +45 53504530 Date Prepared Trade Name Common Name Regulation Name Regulation Number Class Product Code Predicate Device February 8, 2023 ARTSMedia In Vitro Culture Medium (AM-IVC Medium) Assisted Reproduction Media Reproductive Media and Supplements 21 CFR 884.6180 Class II MQL (Media, Reproductive) K133707 ORIGIO als SAGE 1-StepTM supplemented with Human Serum Albumin The predicate device has not been subject to a designrelated recall. #### Device Description ARTSMedia In Vitro Culture Medium (AM-IVC Medium) is a medium for in vitro fertilization and culture of human gametes and embryos from fertilization until the blastocyst stage of development (day 5). The medium can also be used for embryo transfer procedures. The medium is aseptically filtered and provided in in a volume of 10 mL in pre-sterilized 10 mL glass bottles closed with Fluorotec-coated stoppers and aluminum caps. The medium has a shelflife of 10 months when stored at 2-8℃ and is for single-use only. Additional information on the formulation and specifications of AM-IVC Medium are provided in the Comparison of the Subject and Predicate Device Intended Use and Technological Characteristics section of this summary. #### Indications for Use ARTSMedia In Vitro Culture Medium (AM-IVC Medium) is a culture medium intended for in vitro fertilization and in vitro culture of human gametes and embryos from fertilization until the blastocyst stage of development (day 5). The medium can also be used for embryo transfer. {4}------------------------------------------------ ### Comparison of the Subject and Predicate Device Intended Use and Technological Characteristics A comparison of the intended use and technological characteristics of the subject and predicate devices are shown in the table below: | Parameters | K220715 | K133707 | Comparison | |--------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | AM-IVC Medium | SAGE 1-StepTM | | | | Subject Device | Predicate Device | | | Indications for Use | ARTSMedia In Vitro Culture Medium (AM-IVC Medium) is a culture medium intended for in vitro fertilization and in vitro culture of human gametes and embryos from fertilization until the blastocyst stage of development (day 5). The medium can also be used for embryo transfer. | This product is intended for the in vitro fertilization and culture of human gametes and embryos from fertilization until Day 5/6 of development. The media can also be used for embryo transfer. | The subject device indications for use statement is not identical to the predicate device, as it is only for use up to day 5 of development. However, the overall intended use of the subject and predicate device is the same (i.e., for fertilization and culture of embryos to the blastocyst stage of development and for use in embryo transfer procedures). | | Conditions for Use | Prescription Use Only | Prescription Use Only | Same | | Formulation | Physiological Salts Amino Acids Vitamins Calcium Lactate EDTA Gentamicin Sulphate Glucose L-glutamine Human Serum Albumin (HSA) Sodium Bicarbonate Sodium Hyaluronate Sodium Pyruvate Phenol Red Selenite Ethanolamine Sodium citrate Human Insulin (from yeast) | Physiological Salts Amino Acids Calcium -L-Lactate EDTA Gentamicin Sulphate Glucose L-glutamine Human Serum Albumin (HSA) Sodium Bicarbonate Sodium Hyaluronate Sodium Pyruvate Phenol Red | Different: The formulations of the subject and predicate devices are not the same. Differences in device formulations do not raise different questions of safety and effectiveness (S&E). | | Sterilization | Aseptic filtration | Aseptic filtration | Same | | Sterility | No growth | No growth | Same | | pH | 7.2-7.45 | 7.2-7.4 | Similar | | Osmolality (mOsm/kg) | 257-275 | 257-273 | Similar | | Mouse Embryo Assay (MEA) | 1-cell Mouse Embryo Assay (MEA) ≥ 80% embryos developed to expanded blastocysts at 96 hours. | 1-cell MEA ≥ 80% | Similar | | Endotoxin (EU/ml) | <0.05 | <0.15 | Different: The subject device has a lower endotoxin level than the predicate device. This difference in endotoxin specification does not raise different questions of S&E. | | Shelf life | 10 months | 14 weeks | Different: The subject device has a longer shelf-life than the predicate device. Differences in shelf-life do not raise different questions of S&E. | {5}------------------------------------------------ As shown in the table above, there are differences in the indications for use statements and technological characteristics of the subject and predicate devices. However, as stated in the table, the differences in indications for use do not represent a new intended use and the differences in technological characteristics do not raise different questions of safety and effectiveness. #### Summary of Non-Clinical Performance Testing The following studies have been performed to support substantial equivalence to the predicate device: - Biocompatibility testing was conducted in support of the subject device that will have direct . contact with the patient during embryo transfer procedures. Testing was conducted in accordance with the 2020 FDA guidance Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices - Part 1: Evaluation and testing within a risk management process. Testing included: - Cytotoxicity per ISO 10993-5:2009 - - Sensitization per ISO 10993-10:2010 - - -Vaginal Irritation per ISO 10993-10:2010 The testing demonstrated the device formulation to be non-cytotoxic, non-sensitizing, and non-irritating. - . Aseptic filtration and aseptic filling validation, per ISO 13408-1:2008 & A1:2013 and ISO 13408- 2:2018. {6}------------------------------------------------ - Shelf-life testing was conducted to support a 10-month shelf-life for the subject device . through demonstration that the product specifications (shown below) were met at time 0 and after 10 months of real-time aging: - Appearance: Clear and particulate free - - pH, per USP <791>: 7.2-7.45 - Osmolality, per USP <785>: 257-275 mOsm/kg - - Endotoxin, per USP <85>: < 0.05 EU/mL । - MEA testing, in accordance with the 2021 FDA guidance Mouse Embryo Assay for । Assisted Reproduction Technology Devices: 1-Cell Mouse Embryo Assay (MEA) ≥80% embryos developed to expanded blastocyst at 96 hours. - Sterility, per USP <71>: No growth - - . Transportation testing per ASTM D4169-22 and cap/seal leak testing using a method equivalent to USP <1207.2> on transportation-conditioned devices. #### Conclusions The results of the performance testing described above demonstrate that AM-IVC Medium is as safe and effective as the predicate device and supports a determination of substantial equivalence.