Data / Medical devices / United States / Reliance Dental MFG., LLC
Reliance Dental MFG., LLC: FDA-registered device maker in Alsip, IL, United States, 2 510(k) clearances
Reliance Dental MFG., LLC is registered with the FDA (registration 1415367) in Alsip, IL, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 26, 2011. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1415367
- Address
- 5805 West 117th Place, Alsip, IL, United States, 60803
- Owner or operator
- Reliance Dental Mfg., LLC (10048563)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- January 27, 2015
- Registered through
- 2027
- Brand names listed
- DuraConditioner, Dura Rely-A-Soft, DuraSplint, Duralay Plastic Pins, Duralay, Duralay Crown and Bridge, Duralay II, Duraseal, Durabase, Durabase Soft, Duraliner II, Duratray, Trays, Perforated Impression
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Material, Impression Tray, Resin | EBH | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mouthguard, Prescription | MQC | U | Repackager or relabeler | accessdata.fda.gov |
| Post, Root Canal | ELR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Manufacturer | accessdata.fda.gov |
| Tray, Impression, Preformed | EHY | 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 26, 2011 | K111828 | CLEARSPLINT ES | MQC | Substantially Equivalent | Astron Dental Corporation | accessdata.fda.gov |
| September 23, 1985 | K852741 | DURA CONDITIONER | EBI | Substantially Equivalent | Reliance Dental Mfg. Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Material, Impression Tray, Resin
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Mouthguard, Prescription
- All makers of Post, Root Canal
- All makers of Tray, Impression, Preformed
Updated October 26, 2011. 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.