Techno-Path Manufacturing , Ltd.
Techno-Path Manufacturing , Ltd. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2025, with 5 FDA device recalls on record.
Top product codes for Techno-Path Manufacturing , Ltd.
FDA recalls by Techno-Path Manufacturing , Ltd.
- Z-0502-2026 — Multichem ID-B. Model Number: SR103B. Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen and anti-Treponema pallidum IgG.
- Z-0501-2026 — Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen and anti-Treponema pallidum IgG.
- Z-0104-2024 — Multichem S Plus, Part Codes: a) 08P88-10, b) 08P88-11, c) 08P88-12
- Z-0105-2024 — Multichem IA Plus, Part Codes: a) 08P86-10, b) 08P86-19
- Z-0106-2024 — Multichem P, Part Code 08P90-10
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 Techno-Path Manufacturing , Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.