Ki Mobility, LLC: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Ki Mobility, LLC” (first 2006, latest 2023), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 281 days. Since 2017 the median was 718 days, against 124 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 4 | 718 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Ki Mobility, LLC took a median 718 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 124 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| IOR | Wheelchair, Mechanical | 3 | 3 |
| ITI | Wheelchair, Powered | 1 | 1 |
| LBE | Stroller, Adaptive | 1 | 1 |
Review panels
Most recent Ki Mobility, LLC 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K201869 | Ki Power Tilt System | ITI | 2023-09-05 | 1155 |
| K200583 | Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL | IOR | 2023-09-05 | 1278 |
| K223533 | Little Wave Arc; Little Wave Flip | LBE | 2023-08-31 | 281 |
| K223527 | Little Wave Clik, Rogue XP, Little Wave XP, Spark | IOR | 2023-08-31 | 281 |
| K062660 | CATALYSY | IOR | 2006-10-24 | 47 |
Recalls
1 product recalls in 1 recall events; 1 initiated in the last five years. Most recent: 2021-11-19.
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 Ki Mobility, LLC?
FDA lists 5 510(k) clearances under the applicant name “Ki Mobility, LLC” (first 2006, latest 2023), across 3 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Ki Mobility, LLC?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ki Mobility, LLC is 281 days. Since 2017: 718 days, versus 124 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Ki Mobility, LLC?
The most frequent FDA product codes under this applicant name are IOR (Wheelchair, Mechanical, 3); ITI (Wheelchair, Powered, 1); LBE (Stroller, Adaptive, 1).
Next steps
- See all 5 Ki Mobility, LLC clearances with predicates and recalls
- Run predicate analysis for product code IOR, Ki Mobility, LLC'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.