American Dental Products, Inc.
Bensenville, IL, US
American Dental Products, Inc. appears in FDA device records in Bensenville, IL. FDA records list 23 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 23
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 23 510(k) clearances for American Dental Products, Inc. between 1995 and 2010. The busiest year on record is 1995, with 18. The most recent is 2010, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 18 |
| 1997 | 2 |
| 1999 | 1 |
| 2000 | 1 |
| 2010 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K093014 | AMERICAN DENTAL PRODUCTS SE BONDEASY | KLE | Substantially Equivalent | |
| K994368 | AMERICAN DENTAL PRODUCTS CARIES-DETECTOR PLUS | LFC | Substantially Equivalent | |
| K991099 | AMERICAN DENTAL PRODUCTS ETCH-DETECT | EBC | Substantially Equivalent | |
| K973185 | AMERICAN DENTAL PRODUCTS HB-35 DESENSITIZER WITH FLUORIDE | KLE | Substantially Equivalent | |
| K964133 | AMERICAN DENTAL PRODUCTS HG 35 DESENSITIZER WITH FLUORIDE | KLE | Substantially Equivalent | |
| K954637 | AMERICAN DENTAL PRODUCTS TISSUE CONDITIONER & TEMPORARY RELINER | EBI | Substantially Equivalent | |
| K954876 | AMERICAN DENTAL PRODUCTS ROOT CANAL SEALER, WACH'S FORMULA | EMA | Substantially Equivalent | |
| K954701 | AMERICAN DENTAL PRODUCTS PIT & FISSUE SEALANT LIGHT CURING | EBC | Substantially Equivalent | |
| K954408 | AMERICAN DENTAL PRODUCTS LIGHT ACTIVATED COMPOSITE RESIN CORE BUILDUP BLUE PASTEE | EBF | Substantially Equivalent | |
| K954407 | AMERICAN DENTAL PRODUCTS WHITE COMPOSITE RESIN CORE PASTE WITH FLUORIDE | EBF | Substantially Equivalent | |
| K954406 | AMERICAN DENTAL PRODUCTS COMPOSITE RESIN CORE PASTE WITH FLUORIDE | EBF | Substantially Equivalent | |
| K954405 | AMERICAN DENTAL PRODDUCTS LIGHT ACTIVATED COMPOSITE RESIN CORE PASTE WITH FLUORIDE | EBF | Substantially Equivalent | |
| K954133 | AMERICAN DENTAL PRODUCTS WETTING AGENT & DESENSITIZER | KLE | Substantially Equivalent | |
| K954374 | AMERICAN DENTAL PRODUCTS ORTHODONTIC ADHESIVE, TWO PASTE BONDING SYSTEM | DYH | Substantially Equivalent | |
| K954373 | AMERICAN DENTAL PRODUCTS PASTE-PRIMER ADHESIVE ORTHODONTIC BONDING SYSTEM W/FLUORIDE | DYH | Substantially Equivalent | |
| K954372 | AMERICAN DENTAL PRODUCTS TWO PASTE ADHESIVE ORTHODONTIC BONDING SYSTEM W/FLUORIDE | DYH | Substantially Equivalent | |
| K954461 | AMERICAN DENTAL PRODUCTS CORE BUILDUP PASTE | EBF | Substantially Equivalent | |
| K954333 | AMERICAN DENTAL PRODUCTS ORTHODONTIC ADHESIVE W/ONE STEP BONDING SYSTEM | DYH | Substantially Equivalent | |
| K954244 | AMERICAN DENTAL PRODUCTS LIGHT ACTIVATED ORTHODONTIC ADHESIVE BONDING SYSTEM W/FLUORIDE | DYH | Substantially Equivalent | |
| K954223 | AMERICAN DENTAL PRODUCTS ALGINATE FLAVORING | ELW | Substantially Equivalent | |
| K951427 | AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL | EBF | Substantially Equivalent | |
| K951426 | AMERICAN DENTAL PRODUCTS (ADP), VISIBLE LIGHT CURE COMPOSITE DENTAL RESTORATIVE MATERIAL | EBF | Substantially Equivalent | |
| K950512 | AMERICAN DENTAL PRODUCTS (ADP), FLUORIDE RELEASING GLASS IONOMER BAND CEMENT | DYH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain