Time Medical Limited: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Time Medical Limited” (first 2009, latest 2023), across 1 product code in 1 review panel. Median 510(k) review time under this name: 102 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 |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 1 | 58 |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 1 | 208 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Time Medical Limited took a median 133 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 101 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LNH | System, Nuclear Magnetic Resonance Imaging | 6 | 6 |
Review panels
- Radiology (6)
Most recent Time Medical Limited 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K222259 | NEONA 1.5T MRI System | LNH | 2023-02-21 | 208 |
| K183621 | EMMA 1.5T MRI System | LNH | 2019-02-22 | 58 |
| K110942 | PICA WHOLE-BODY MRI SYSTEM | LNH | 2011-07-26 | 113 |
| K093984 | PICA WHOLE BODY MRI SYSTEM MODEL TMS-MRI-3500WB-01 | LNH | 2010-03-24 | 90 |
| K092230 | MONA - ORTHOPEDIC MRI SYSTEM, MODEL TMS-200ORTH-01 | LNH | 2009-11-25 | 125 |
| K091580 | PICA WHOLE BODY MRI SYSTEM | LNH | 2009-07-24 | 52 |
Recalls
openFDA lists no recalls under a recalling firm named Time Medical Limited.
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.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Time Medical Limited (a text match, not an official crosswalk):
- C8903 — Magnetic resonance imaging with contrast, breast; unilateral (via LNH)
- C8906 — Magnetic resonance imaging with contrast, breast; bilateral (via LNH)
- C8905 — Magnetic resonance imaging without contrast followed by with contrast, breast; unilateral (via LNH)
- C8908 — Magnetic resonance imaging without contrast followed by with contrast, breast; bilateral (via LNH)
- C8900 — Magnetic resonance angiography with contrast, abdomen (via LNH)
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.
- Time Motion System Co. (2 510(k)s)
- Time Computer, Inc. (Tci) (1 510(k)s)
- Time IS Brain, S.L. (1 510(k)s)
- Time Medical Systems, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Time Medical Limited?
FDA lists 6 510(k) clearances under the applicant name “Time Medical Limited” (first 2009, latest 2023), 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 Time Medical Limited?
The median time from FDA receipt to decision across 510(k)s cleared under the name Time Medical Limited is 102 days.
Which FDA product codes appear under Time Medical Limited?
The most frequent FDA product codes under this applicant name are LNH (System, Nuclear Magnetic Resonance Imaging, 6).
Next steps
- See all 6 Time Medical Limited clearances with predicates and recalls
- Run predicate analysis for product code LNH, Time Medical Limited'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.