Data / Medical devices / Germany / Lohmann & Rauscher GMBH & Co. KG
Lohmann & Rauscher GMBH & Co. KG: FDA-registered device maker in NEUWIED Rhineland-Palatinate, Germany, 1 510(k) clearance
Lohmann & Rauscher GMBH & Co. KG is registered with the FDA (registration 9611462) in NEUWIED Rhineland-Palatinate, Germany. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 1980. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9611462
- FEI number
- 3002807486
- Address
- Irlicher Strasse 55, NEUWIED Rhineland-Palatinate, Germany, 56567
- Owner or operator
- LOHMANN & RAUSCHER GMBH & CO. KG (8010825)
- Roles
- Manufacturer, Specification developer
- First device listed
- February 14, 1994
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Cast | ITG | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Dressing, Compression | MHW | 1 | Specification developer | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Specification developer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Specification developer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Manufacturer | accessdata.fda.gov |
| Sponge, Ophthalmic | HOZ | 2 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | 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 22, 1980 | K802794 | PRO-OPHTA STICKS | HOZ | Substantially Equivalent | Secol Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Protector, Skin Pressure
- All makers of Dressing, Wound, Occlusive
- All makers of Dressing, Compression
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Bandage, Elastic
- All makers of Dressing, Wound, Hydrophilic
Updated December 22, 1980. 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.