Amo Manufacturing USA, LLC
Amo Manufacturing USA, LLC holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2023, with 2 FDA device recalls on record.
Top product codes for Amo Manufacturing USA, LLC
FDA recalls by Amo Manufacturing USA, LLC
- Z-0444-2022 — Catalys Precision Laser System, Models: Catalys-U (United States), Catalys-I (International), Catalys-C (China); and Catalys Precision Laser System No Bed, Models: 0160-6020 (United States), 0160-6010 (International)
- Z-0443-2022 — iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States); iDesign Refractive Studio Aberrometer (International) and (United States), Model: G301
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 Amo Manufacturing USA, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.