FDA applicant

Spectrum Co.

Los Angeles, CA3 decisions1982–19890 recalls

FDA records 3 decisions for Spectrum Co. (Los Angeles, CA) from 1982 to 1989: 3 510(k) clearances. Most are in product codes JSM (Culture Media, Non-Propagating Transport) and HHT (Spatula, Cervical, Cytological). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Spectrum Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Spectrum Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Spectrum Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Spectrum”

FDA records each applicant name separately; these may or may not be the same firm.

Spectrum Medical, Ltd. 23 Spectrum Designs, Inc. 18 Spectrum X-Ray Corp. 9 Spectrum Dynamics Medical, Ltd. 8 Spectrum Spine, LLC 8 Spectrum Vascular 6 Spectrum Medical Technologies, Inc. 3 Spectrum Diagnostic, Inc. 3 Spectrum Dynamics, Ltd. 3 Spectrum Antimicrobials, Inc. 1 Spectrum Antimicrobials, Inc. (Subsidiary of… 1 Spectrum Spine IP Holdings, LLC 1

Spectrum Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Spectrum”