Data / Medical devices / United States / Addition Technology, Inc.
Addition Technology, Inc.: FDA-registered device maker in Lombard, IL, United States, 1 PMA approval
Addition Technology, Inc. is registered with the FDA (registration 2953726) in Lombard, IL, United States. It lists 7 device types. The FDA files 1 PMA approval under its listings, the newest dated April 9, 1999. 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
- 2953726
- FEI number
- 3000309468
- Address
- 820 Oak Creek Dr, Lombard, IL, United States, 60148
- Owner or operator
- Addition Technology (9099993)
- Roles
- Manufacturer, Manufacturer for export
- First device listed
- May 18, 1999
- Registered through
- 2026
- Brand names listed
- 11200-210/300-150, ICIA-210/300-150, Intacs Corneal Implants, Asymmetric Treatment 0.210mm/0.300mm, 11200-210/350-150, ICIA-210/350-150, Intacs Corneal Implants, Asymmetric Treatment 0.210mm/0.350mm, 11200-210/400-150, ICIA-210/400-150, Intacs Corneal Implants, Asymmetric Treatment 0.210mm/0.400mm, 11200-210/450-150, ICIA-210/450-150, Intacs Corneal Implants, Asymmetric Treatment 0.210mm/0.450mm, 11400-210/300-150, ICIA-210/300-150, Intacs Corneal Implants, Asymmetric 0.210mm/0.300mm, 11400-210/350-150, ICIA-210/350-150, Intacs Corneal Implants, Asymmetric 0.210mm/0.350mm, 11400-210/400-150, ICIA-210/400-150, Intacs Corneal Implants, Asymmetric 0.210mm/0.400mm, 11400-210/450-150, ICIA-210/450-150, Intacs Corneal Implants, Asymmetric 0.210mm/0.450mm and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Forceps, Ophthalmic | HNR | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Corneal, Refractive | LQE | 3 | Manufacturer, Manufacturer for export | accessdata.fda.gov |
| Marker, Ocular | HMR | 1 | Manufacturer | accessdata.fda.gov |
| Ring, Ophthalmic (Flieringa) | HNH | 1 | Manufacturer | accessdata.fda.gov |
| Rongeur, Lachrymal Sac | HNG | 1 | Manufacturer | accessdata.fda.gov |
| Spatula, Ophthalmic | HND | 1 | Manufacturer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| April 9, 1999 | P980031 | INTACS PRESCRIPTION INSERTS/INTACS CORNEAL IMPLANTS | LQE | 13 | May 2, 2025 | accessdata.fda.gov |
Compare with other makers
- All makers of Rongeur, Lachrymal Sac
- All makers of Forceps, Ophthalmic
- All makers of Spatula, Ophthalmic
- All makers of Ring, Ophthalmic (Flieringa)
- All makers of Tubing, Noninvasive
Updated May 2, 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.