Soring GmbH Medizintechnik: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Soring GmbH Medizintechnik” (first 1999, latest 2010), across 4 product codes in 1 review panel. Median 510(k) review time under this name: 58 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 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 4 | 4 |
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 1 | 1 |
| LFL | Instrument, Ultrasonic Surgical | 1 | 1 |
| QPB | System, Suction, Lipoplasty For Removal | 1 | 1 |
Review panels
Most recent Soring GmbH Medizintechnik 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K093511 | SORING MBC200/BCC140 | GEI | 2010-04-16 | 154 |
| K052183 | SORING GMBH SONOCA LIPO | QPB | 2005-10-07 | 58 |
| K030028 | CPC BY SORING GMBH | GEI | 2003-01-17 | 14 |
| K024059 | MBC SERIES | GEI | 2003-01-08 | 30 |
| K012753 | SORING GMBH SONOCA 180/190 | LFL | 2001-11-13 | 89 |
| K993265 | SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 | GEI | 1999-10-22 | 23 |
| K992026 | SORING GMBH, SONOCA 300 | BTA | 1999-09-23 | 99 |
Recalls
openFDA lists no recalls under a recalling firm named Soring GmbH Medizintechnik.
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 Soring GmbH Medizintechnik?
FDA lists 7 510(k) clearances under the applicant name “Soring GmbH Medizintechnik” (first 1999, latest 2010), across 4 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 Soring GmbH Medizintechnik?
The median time from FDA receipt to decision across 510(k)s cleared under the name Soring GmbH Medizintechnik is 58 days.
Which FDA product codes appear under Soring GmbH Medizintechnik?
The most frequent FDA product codes under this applicant name are GEI (Electrosurgical, Cutting & Coagulation & Accessories, 4); BTA (Pump, Portable, Aspiration (Manual Or Powered), 1); LFL (Instrument, Ultrasonic Surgical, 1).
Next steps
- See all 7 Soring GmbH Medizintechnik clearances with predicates and recalls
- Run predicate analysis for product code GEI, Soring GmbH Medizintechnik'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.