Data / Medical devices / Taiwan / Geon Corporation
Geon Corporation: FDA-registered device maker in CHANG HWA HSIEN Changhua, Taiwan, 4 510(k) clearances
Geon Corporation is registered with the FDA (registration 9680961) in CHANG HWA HSIEN Changhua, Taiwan. It lists 5 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 4, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680961
- FEI number
- 3005479955
- Address
- No. 12, Gung Ye Road Hsi Hu, CHANG HWA HSIEN Changhua, Taiwan, 514
- Owner or operator
- Geon Corporation (9012605)
- Roles
- Manufacturer
- First device listed
- December 7, 2008
- Registered through
- 2026
- Brand names listed
- ADTEMP ADIMAL DIG. THERMOMETER DUAL SCALE, GEON BASAL THERMOMETER MODEL:MT-B221, MT-B231, MT-B231A, MT-B231F, MT-B261, MT-B261A, MT-B263, MT-B263A, MT-B281,MT-OR2, GEON DIGITAL CLINICAL THERMOMETER#:MT-B122,MT-B132,MT-B132A,MT-B132F,MT-B162,MT-B162A,MT-B163,MT-B163A,MT-B182,MT-B120,MT-B1708,MT-OR, GEON DIGITAL THERMOMETER SHEATHS, GEON EAR THERMOMETER MODEL NO.: GE-TE06, GE-TE07, GE-TE09, GE-TE07A, GE-TE09A, GE-TE07+, GE-TE09+, GE-TE07A+, GE-TE09A+, GEON EAR THERMOMETER PROBE COVERS, GEON FOREHEAD THERMOMETER MODEL NO.: GE-TF02, GE-TF03, GE-TF11, GE-TF12, GE-TF13, GEON INSTANT DIGITAL THERMOMETER Model No.: MT-F117, MT-F127, MT-F130, MT-F132FB, MT-F1010F, MT-F1010FP, MT-F1251, MT-F2251 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Clinical Electronic Thermometer | SDV | 2 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Irrigator, Powered Nasal | KMA | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 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 |
|---|---|---|---|---|---|---|
| February 4, 2025 | K243138 | Geon (S2) Nasal Aspirator | BTA | Substantially Equivalent | Geon Corporation | accessdata.fda.gov |
| February 2, 2023 | K220126 | Geonic Nasal Aspirator, Geonic Nasal Cleaner | BTA | Substantially Equivalent | Geon Corporation | accessdata.fda.gov |
| June 2, 2010 | K100563 | GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FA | FLL | Substantially Equivalent | Geon Corporation | accessdata.fda.gov |
| January 12, 2001 | K003223 | GEON DIGITAL CLINICAL THERMOMETER | FLL | Substantially Equivalent | Geon Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Clinical Electronic Thermometer
- All makers of Irrigator, Powered Nasal
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Continuous Measurement Thermometer
- All makers of Bottle, Collection, Vacuum
Updated February 4, 2025. 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.