Active Life Scientific, Inc.: FDA filings under this applicant name
FDA lists 2 510(k) clearances under the applicant name “Active Life Scientific, Inc.” (first 2022, latest 2025), plus 1 De Novo decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 147 days. 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 |
|---|---|---|
| 2022 | 1 | 64 |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 1 | 230 |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Active Life Scientific, Inc. took a median 147 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 147 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| QGQ | Bone Indentation Device | 3 | 2 |
Review panels
- Orthopedic (3)
Most recent Active Life Scientific, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K250216 | OsteoProbe (OP-100) | QGQ | 2025-09-11 | 230 |
| K221195 | OsteoProbe | QGQ | 2022-06-28 | 64 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| DEN210013 | De Novo | Bone Indentation Device | 2021-08-19 |
Recalls
openFDA lists no recalls under a recalling firm named Active Life Scientific, 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.
Device clinical trials
An industry sponsor named Active Life Scientific, Inc. is the lead sponsor of 1 device studies on ClinicalTrials.gov (0 active or recruiting). Most recent:
- NCT04628221: Open Label Study Using OsteoProbe System (Completed, started 2020-07-31)
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Active Electronics, Inc. (7 510(k)s)
- Active Vertical Correctors, Inc. (2 510(k)s)
- Active Corp. (1 510(k)s)
- Active Optical Systems , Ltd. (1 510(k)s)
- Active Optical Systems, Ltd./Efraim Bidas (1 510(k)s)
- Active Signal Technologies, Inc. (1 510(k)s)
- Active Protective Technologies, Inc. (0 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Active Life Scientific, Inc.?
FDA lists 2 510(k) clearances under the applicant name “Active Life Scientific, Inc.” (first 2022, latest 2025), plus 1 De Novo decision, across 1 product code 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 Active Life Scientific, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Active Life Scientific, Inc. is 147 days.
Which FDA product codes appear under Active Life Scientific, Inc.?
The most frequent FDA product codes under this applicant name are QGQ (Bone Indentation Device, 3).
Next steps
- See all 2 Active Life Scientific, Inc. clearances with predicates and recalls
- Run predicate analysis for product code QGQ, Active Life Scientific, 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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.