Pear Therapeutics, Inc.
Pear Therapeutics, Inc. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Pear Therapeutics, Inc.
FDA recalls by Pear Therapeutics, Inc.
- Z-1925-2021 — reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
- Z-1926-2021 — reSET-O Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Pear Therapeutics, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.