FDA applicant
Dr. Bruno Lange GmbH
FDA records 5 decisions for Dr. Bruno Lange GmbH (Mchenry, IL) from 1980 to 1984: 5 510(k) clearances. Most are in product codes JJQ (Colorimeter, Photometer, Spectrophotometer For…) and JJO (Flame Emission Photometer For Clinical Use). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Dr. Bruno Lange GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dr. Bruno Lange GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dr. Bruno Lange GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report