Rls Global AB: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Rls Global AB”, plus 1 PMA decision, across 1 product code in 1 review panel. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LMW | Solution, Removal, Carries | 1 | 0 |
Review panels
- Dental (1)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P000005 | PMA | CARISOLV NON-INVASIVE DENTAL CARIES REMOVAL SYSTEM | 2001-06-27 |
Recalls
openFDA lists no recalls under a recalling firm named Rls Global AB.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Rls Global AB?
FDA lists 0 510(k) clearances under the applicant name “Rls Global AB”, plus 1 PMA decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Rls Global AB?
The most frequent FDA product codes under this applicant name are LMW (Solution, Removal, Carries, 1).
Next steps
- See all 0 Rls Global AB clearances with predicates and recalls
- Run predicate analysis for product code LMW, Rls Global AB's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.