Data / Medical devices / United States / Anthony Products, Inc.
Anthony Products, Inc.: FDA-registered device maker in Indianapolis, IN, United States, 1 510(k) clearance
Anthony Products, Inc. is registered with the FDA (registration 1824037) in Indianapolis, IN, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 19, 2000. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 1824037
- Address
- 7740 Records ST, Indianapolis, IN, United States, 46226
- Owner or operator
- Anthony Products, Inc. (10025507)
- Roles
- Repackager or relabeler
- First device listed
- February 5, 2013
- Registered through
- 2026
- Brand names listed
- GEAC TIP
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| October 19, 2000 | K002257 | TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 | GEI | Substantially Equivalent | Tecno Instruments (Pvt.) , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Scissors, General, Surgical
Updated October 19, 2000. 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.