Data / Medical devices / Laryngoscope, Nasopharyngoscope
Laryngoscope, Nasopharyngoscope (EQN): 10 FDA-registered makers in 3 countries
10 establishments in 3 countries are registered with the FDA to make Laryngoscope, Nasopharyngoscope (product code EQN, Class 2, 21 CFR 874.4760). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 22 510(k) clearances under this code, the latest on May 15, 2026, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- EQN
- Device class
- 2
- Regulation
- 874.4760
- Medical specialty
- Ear, Nose, Throat
Makers by country
| Country | Makers |
|---|---|
| Germany | 5 |
| United States | 4 |
| Japan | 1 |
Makers of Laryngoscope, Nasopharyngoscope
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| It Concepts GMBH | Lahnau Hesse, Germany | Manufacturer | 1 | July 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| JEDMED Instrument Company | Saint Louis, MO, United States | Manufacturer, Repackager or relabeler | 1 | May 13, 1982 | 0 | 0 | 0 | api.fda.gov |
| Karl Storz Se & Co KG | TUTTLINGEN Baden-Wurttemberg, Germany | Specification developer | 1 | May 15, 2026 | 0 | 0 | 0 | api.fda.gov |
| Machida Endoscope Co., Ltd. | Abiko Chiba, Japan | Manufacturer | 1 | May 13, 1982 | 0 | 0 | 0 | api.fda.gov |
| Orlvision GMBH | Lahnau Hesse, Germany | Contract manufacturer, Manufacturer | 1 | July 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 1 | January 21, 1977 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 1 | January 21, 1977 | 0 | 0 | 0 | api.fda.gov |
| Harwood Design, Inc. | Bristol, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 15, 2026. 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.