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Food and Drug Administration, HHS.
Notice of availability.
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance entitled “Regulatory Considerations for Microneedling Products.” This guidance is being issued to assist industry in understanding when a microneedling product is a device as defined in the Federal Food, Drug, and Cosmetic Act (FD&C Act). This document also provides information on the regulatory pathway to market for microneedling devices for aesthetic use.
The announcement of the guidance is published in the Federal Register on November 10, 2020.
You may submit either electronic or written comments on Agency guidances at any time as follows:
Submit electronic comments in the following way:
Submit written/paper submissions as follows:
Instructions: All submissions received must include the Docket No. FDA-2017-D-4792 for “Regulatory Considerations for Microneedling Products.” Received comments will be placed in the docket and, except for those submitted as “Confidential Submissions,” publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday, 240-402-7500. ( printed page 71657)
Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the “Search” box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240-402-7500.
You may submit comments on any guidance at any time (see 21 CFR 10.115(g)(5)).
An electronic copy of the guidance document is available for download from the internet. See the SUPPLEMENTARY INFORMATION section for information on electronic access to the guidance. Submit written requests for a single hard copy of the guidance document entitled “Regulatory Considerations for Microneedling Products” to the Office of the Center Director, Guidance and Policy Development, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5431, Silver Spring, MD 20993-0002. Send one self-addressed adhesive label to assist that office in processing your request.
Kimberly Ferlin, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 4522, Silver Spring, MD 20993-0002, 240-402-1834.
“Microneedling products” is a generic term that encompasses instruments with common technological features that include an array of needles, “micro-protrusion” tips, or pins, which can be blunt or sharp, and of varying lengths. This document discusses when a microneedling product is a device as defined under section 201(h) of the FD&C Act (21 U.S.C. 321(h)), and is, therefore, subject to the device requirements under the FD&C Act and its implementing regulations.[1] This guidance also provides clarity on the regulatory pathway to market for microneedling devices for aesthetic use, resulting in more transparency and predictability to firms and stakeholders, which may translate into more efficient device development and patient access to such devices. The scope of this guidance document does not include microneedling combination products, acupuncture needles, hypodermic needles or other needles for injection, tattoo machine needles, needle probes that emit any type of energy ( e.g., radio-frequency needles) or deliver any type of energy to a patient ( e.g., LASER, ultrasound), or dermabrasion devices. FDA considered comments received on the draft guidance that appeared in the Federal Register of September 15, 2017 (82 FR 43383). FDA revised the guidance as appropriate in response to the comments. Further, the guidance was revised to account for a De Novo request that was granted since issuance of the draft, which classified microneedling devices for aesthetic use into class II subject to premarket notification requirements under section 510(k) of the FD&C Act ((21 U.S.C. 360(k)) and special controls. The classification is codified at 21 CFR 878.4430.
This guidance is being issued consistent with FDA's good guidance practices regulation (21 CFR 10.115). The guidance represents the current thinking of FDA on “Regulatory Considerations for Microneedling Products.” It does not establish any rights for any person and is not binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the applicable statutes and regulations.
Persons interested in obtaining a copy of the guidance may do so by downloading an electronic copy from the internet. A search capability for all Center for Devices and Radiological Health guidance documents is available at https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/default.htm. This guidance document is also available at https://www.regulations.gov and at https://www.fda.gov/regulatory-information/search-fda-guidance-documents. Persons unable to download an electronic copy of “Regulatory Considerations for Microneedling Products” may send an email request to CDRH-Guidance@fda.hhs.gov to receive an electronic copy of the document. Please use the document number 1500036 to identify the guidance you are requesting.
While this guidance contains no collection of information, it does refer to previously approved FDA collections of information. Therefore, clearance by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-3521) is not required for this guidance. The previously approved collections of information are subject to review by OMB under the PRA. The collections of information in the following FDA regulations and guidance have been approved by OMB as listed in the following table:
| 21 CFR part; guidance; or FDA form | Topic | OMB control No. |
|---|---|---|
| 807, subpart E | Premarket notification | 0910-0120 |
| ( printed page 71658) | ||
| “De Novo Classification Process (Evaluation of Automatic Class III Designation)” | De Novo classification process | 0910-0844 |
| “Requests for Feedback on Medical Device Submissions: The Pre-Submission Program and Meetings with Food and Drug Administration Staff” | Q-submissions | 0910-0756 |
| 800, 801, and 809 | Medical Device Labeling Regulations | 0910-0485 |
Dated: November 5, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
1. On September 23, 2020, FDA published a proposed rule to amend its intended use regulations for medical products (21 CFR 201.128 and 801.4) to better reflect the Agency's current practices in evaluating whether a product is intended for use as a drug or device. As described in the proposed rule, FDA's longstanding position is that, in evaluating a product's intended use, any relevant source of evidence may be considered, including a variety of direct and circumstantial evidence. 85 FR 59718, 59721 (Sept. 23, 2020).
Back to Citation[FR Doc. 2020-24943 Filed 11-9-20; 8:45 am]
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