FDA applicant
Research Instruments, Ltd.
FDA records 9 decisions for Research Instruments, Ltd. (Falmouth, GB) from 1999 to 2017: 9 510(k) clearances. Most are in product codes MQH (Microtools, Assisted Reproduction (Pipettes)) and MRX (System, Assisted Reproduction Laser). Its devices cite 9 predicates, 4 of them its own earlier devices. 2 recalls are linked to its devices.
FDA’s records also spell it “Research Instruments Limited”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Research Instruments, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
1in 2019
Class I Class II/III not classified
Planning a device like Research Instruments, Ltd.’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) ReportOther applicant names beginning “Research”
FDA records each applicant name separately; these may or may not be the same firm.