Lccs Products Limited: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Lccs Products Limited” (first 2011, latest 2020), across 3 product codes in 3 review panels. Median 510(k) review time under this name: 239 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 | 2 | 148 |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 1 | 346 |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 1 | 255 |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Lccs Products Limited took a median 255 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 116 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GXI | Probe, Radiofrequency Lesion | 3 | 3 |
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | 1 | 1 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1 | 1 |
Review panels
Most recent Lccs Products Limited 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K191293 | LCCS VC-S RF Cannula | GXI | 2020-01-24 | 255 |
| K152642 | LCCS Disposable RF Electrode, LCCS Reusable RF Electrode | GXI | 2016-08-26 | 346 |
| K131006 | ANESTHESIA CONDUCTION NEEDLES | BSP | 2013-12-06 | 239 |
| K132136 | SINGLE USE GROUNDING PAD | GEI | 2013-09-06 | 57 |
| K112231 | LCCS INSULATED SPINAL NEEDLE (RF CANNULA) | GXI | 2011-08-19 | 15 |
Recalls
openFDA lists no recalls under a recalling firm named Lccs Products 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Lccs Products Limited?
FDA lists 5 510(k) clearances under the applicant name “Lccs Products Limited” (first 2011, latest 2020), across 3 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Lccs Products Limited?
The median time from FDA receipt to decision across 510(k)s cleared under the name Lccs Products Limited is 239 days.
Which FDA product codes appear under Lccs Products Limited?
The most frequent FDA product codes under this applicant name are GXI (Probe, Radiofrequency Lesion, 3); BSP (Needle, Conduction, Anesthetic (W/Wo Introducer), 1); GEI (Electrosurgical, Cutting & Coagulation & Accessories, 1).
Next steps
- See all 5 Lccs Products Limited clearances with predicates and recalls
- Run predicate analysis for product code GXI, Lccs Products 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.