Data / Medical devices / Germany / Innoview GMBH
Innoview GMBH: FDA-registered device maker in Eichstetten Baden-Wurttemberg, Germany, 4 510(k) clearances
Innoview GMBH is registered with the FDA (registration 9615001) in Eichstetten Baden-Wurttemberg, Germany. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 8, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9615001
- FEI number
- 3003922255
- Address
- Bruckmatten 35, Eichstetten Baden-Wurttemberg, Germany, D-79356
- Owner or operator
- INNOVIEW GMBH (9026517)
- Roles
- Manufacturer
- First device listed
- June 3, 1997
- Registered through
- 2026
- Brand names listed
- BAHO ARTHROSCOPE, BAHO AUTOCALAVABLE CYSTOSCOPE, BAHO AUTOCLAVABLE LAPAROSCOPE, BAHO OTOSCOPE, Innoview Instrument, RUDOLF INNOVIEW AUTOCLAVABLE SEMI-R
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Arthroscope | HRX | 2 | Manufacturer | accessdata.fda.gov |
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Ent Manual Surgical | LRC | 1 | Manufacturer | accessdata.fda.gov |
| Laparoscope, Gynecologic (And Accessories) | HET | 2 | Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Manufacturer | accessdata.fda.gov |
| Ureteroscope And Accessories, Flexible/Rigid | FGB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 8, 2006 | K062707 | RUDOLF INNOVIEW AUTOCLAVABLE SEMI-RIGID URETERO-RENOSCOPE | FGB | Substantially Equivalent | Innovative Endoscopy Components, LLC | accessdata.fda.gov |
| October 7, 1999 | K992983 | BAHO AUTOCLAVABLE CYSTOSCOPE | FAJ | Substantially Equivalent | Innovative Endoscopy Components, LLC | accessdata.fda.gov |
| February 18, 1999 | K982276 | BAHO AUTOCLAVABLE LAPAROSCOPE | HET | Substantially Equivalent | Microptix Int'L, LLC | accessdata.fda.gov |
| September 11, 1996 | K962330 | AMO ARTHOSCOPES | HRX | Substantially Equivalent | American Microptiks, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cystoscope And Accessories, Flexible/Rigid
- All makers of Ureteroscope And Accessories, Flexible/Rigid
- All makers of Laparoscope, Gynecologic (And Accessories)
- All makers of Instrument, Ent Manual Surgical
- All makers of Arthroscope
- All makers of Otoscope
Updated December 8, 2006. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.