Data / Medical devices / United States / Reliance Orthodontic Products, Inc.
Reliance Orthodontic Products, Inc.: FDA-registered device maker in Itasca, IL, United States, 41 510(k) clearances
Reliance Orthodontic Products, Inc. is registered with the FDA (registration 1420089) in Itasca, IL, United States. It lists 26 device types. The FDA files 41 510(k) clearances under its listings, the newest dated July 20, 2021. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 1420089
- Address
- 1540 West Thorndale Ave., Itasca, IL, United States, 60143
- Owner or operator
- RELIANCE ORTHODONTIC PRODUCTS, INC. (1420089)
- Roles
- Contract manufacturer, Manufacturer for export, Repackager or relabeler, Specification developer
- First device listed
- October 17, 2005
- Registered through
- 2026
- Brand names listed
- 19 GAUGE SYRINGE TIPS (TIPS), A2 Aligner Attachment, ACCESS CHEEK RETRACTOR, Aqua Bond, Assure, BEND A BRUSH, BRUSH HANDLE, BRUSH TIPS and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| July 20, 2021 | K210349 | TKO Composite Bite Turbo Gel | EBF | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| July 8, 2021 | K210945 | Ultra SEP | KLE | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| April 27, 2020 | K193388 | GlassLok Kits, GlassLok Powder, GlassLok Liquid | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| October 6, 2016 | K161684 | Quantum LB | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| April 5, 2013 | K130237 | PONTIC PAINT | NXC | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 28, 2013 | K123348 | CLEAR ALIGNER ADHESIVE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 7, 2012 | K113401 | ORTHO-1(NOT FINALIZED) | DYH | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| November 17, 2011 | K112118 | DREAMBOND | KLE | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| September 14, 2011 | K111814 | PADLOCK | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| October 26, 2010 | K101951 | LIGHT CURE RETAINER | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| August 26, 2010 | K101485 | ALL-ETCH, ALL- ETCH WITH BAC; UNI- ETCH, UNI- ETCH WITH BAC; ETCH- 37, ETCH- 37 WITH BAC; DARK- ETCH, DARK ETCH (BLUE- E | KLE | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| February 20, 2009 | K083051 | FLOWTAIN & FLOWTAIN LV | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 8, 2008 | K073243 | LED PRO SEAL | EBD | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| September 7, 2007 | K071688 | RELIANCE S.E.P. | KLE | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| July 31, 2007 | K071590 | THERMA-CURE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| March 29, 2006 | K052122 | BISCO LED | EBZ | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| April 15, 2003 | K030292 | GROMAN PREPMASTER | KOJ | Substantially Equivalent | Groman, Inc. | accessdata.fda.gov |
| August 1, 2002 | K021503 | UNINHIBITED | EBD | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| April 27, 2000 | K001048 | LIGHT BOND (QUICK CURE) | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| January 3, 1995 | K945604 | ECLIPTOMER | KLE | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| January 21, 1994 | K934405 | PRECEDENT | EMA | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| July 22, 1993 | K932379 | ALL-BOND(R) JR. | KLE | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| March 31, 1993 | K926238 | BISCO PORCELAIN ETCHING GEL | EIH | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| December 28, 1992 | K924151 | BISCO D/C RESINOMER | EBF | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| April 29, 1991 | K910860 | ALL-BOND 2 | KLE | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| December 8, 1989 | K895523 | PHASE II ORTHODONTIC ADHESIVE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| December 7, 1989 | K895522 | LIGHT BOND PASTE W/FLUORIDE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| December 7, 1989 | K895521 | RELY-A-BOND W/FLUORIDE (NO MIX ADHESIVE) | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| October 13, 1989 | K894565 | LIGHT BOND SEALANT WITH FLUORIDE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| September 19, 1989 | K894566 | MAXIMUM CURE SEALANT WITH FLUORIDE | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| June 13, 1988 | K880793 | LIGHT BOND | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| April 25, 1988 | K880766 | RELIANCE METAL PRIMER | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| April 18, 1988 | K880792 | PLASTIC PRIMER | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| April 18, 1988 | K880790 | PORCELAIN PRIMER | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| March 10, 1988 | K875313 | PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST | EBF | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
| February 29, 1988 | K875142 | PHASE II | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 26, 1988 | K875145 | MAR BOND | EBG | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 26, 1988 | K875144 | EXCEL FAST SET | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 26, 1988 | K875143 | RELY-A-BOND(NO MIX ORTHODONTIC ADHESIVE) | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| February 26, 1988 | K875141 | EXCEL REGULAR SET | DYH | Substantially Equivalent | Reliance Orthodontic Products, Inc. | accessdata.fda.gov |
| August 16, 1985 | K853001 | BISFIL-M(LIGHT CURABLE ANTERIOR COMPOSITE) | EBF | Substantially Equivalent | Bisco, Inc. | accessdata.fda.gov |
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Updated July 20, 2021. 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.