Medtimo, Inc.: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Medtimo, Inc.”, plus 2 PMA decisions, 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 |
|---|---|---|---|
| LTI | Implant, Intragastric For Morbid Obesity | 2 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P160001 | PMA | OBALON BALLOON SYSTEM | 2016-09-08 |
| P000008 | PMA | LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM | 2001-06-05 |
Recalls
openFDA lists no recalls under a recalling firm named Medtimo, Inc..
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 Medtimo, Inc.?
FDA lists 0 510(k) clearances under the applicant name “Medtimo, Inc.”, plus 2 PMA decisions, 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 Medtimo, Inc.?
The most frequent FDA product codes under this applicant name are LTI (Implant, Intragastric For Morbid Obesity, 2).
Next steps
- See all 0 Medtimo, Inc. clearances with predicates and recalls
- Run predicate analysis for product code LTI, Medtimo, Inc.'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.