Data / Medical devices / India / Modern Orthodontics
Modern Orthodontics: FDA-registered device maker in Ludhiana, Punjab, India, 2 510(k) clearances
Modern Orthodontics is registered with the FDA (registration 3006237499) in Ludhiana, Punjab, India. It lists 9 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 21, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006237499
- Address
- Hambran Industrial Area,Village Hambran, Ludhiana, Ludhiana, Punjab, India, 141110
- Owner or operator
- MODERN ORTHODONTICS (9105681)
- Roles
- Manufacturer
- First device listed
- August 10, 2007
- Registered through
- 2026
- Brand names listed
- ACE, AccuForm, At-Ease, Sapphire, Sapphire Plus, Micro LP, Curio, Purity-MS, Purity,D'Art, Elegant, ELFIN, AFIX, ElastoSure, Sapphire, At-Ease, Sapphire Plus, Micro LP, TiNol-1 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adhesive, Denture, Karaya | KOP | 1 | Manufacturer | accessdata.fda.gov |
| Band, Elastic, Orthodontic | ECI | 1 | Manufacturer | accessdata.fda.gov |
| Band, Preformed, Orthodontic | ECM | 1 | Manufacturer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Manufacturer | accessdata.fda.gov |
| Bracket, Plastic, Orthodontic | DYW | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Ligature Tucking, Orthodontic | ECP | 1 | Manufacturer | accessdata.fda.gov |
| Spring, Orthodontic | ECO | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Orthodontic | DZD | 1 | Manufacturer | accessdata.fda.gov |
| Wire, Orthodontic | DZC | 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 |
|---|---|---|---|---|---|---|
| November 21, 1997 | K973776 | REFLECTIONS | DYW | Substantially Equivalent | Cdb Corp. | accessdata.fda.gov |
| July 30, 1992 | K922499 | REFLECTIONS - CERAMIC DENTAL BRACKET | EJF | Substantially Equivalent | Cdb Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Bracket, Plastic, Orthodontic
- All makers of Instrument, Ligature Tucking, Orthodontic
- All makers of Tube, Orthodontic
- All makers of Bracket, Metal, Orthodontic
- All makers of Wire, Orthodontic
- All makers of Band, Preformed, Orthodontic
Updated November 21, 1997. 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.