Theralase, Inc.
Theralase, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2015, with 7 FDA device recalls on record.
Top product codes for Theralase, Inc.
FDA recalls by Theralase, Inc.
- Z-1354-2020 — TLC-2000 Therapeutic Medical Laser System
- Z-0607-2020 — TLC-2000 Therapeutic Medical Laser System, Power Pack component TLC-2002 Used for the temporary relief of knee pain.
- Z-1266-2020 — TLC-2000 Therapeutic Medical Laser System
- Z-1348-2020 — TLC-2000 Therapeutic Medical Laser System Power Pack, Model Number TLC-2002
- Z-0606-2020 — TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
- Z-1353-2020 — TLC-2000 Therapeutic Medical Laser System
- Z-1326-2020 — TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for the temporary relief of knee pain.
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 Theralase, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.