KENTEX
Gauze/sponge, Internal
KENTRON HEALTH CARE, INC.
The following data is part of a premarket notification filed by Kentron Health Care, Inc. with the FDA for Kentex.
Pre-market Notification Details
| Device ID | K953914 |
| 510k Number | K953914 |
| Device Name: | KENTEX |
| Classification | Gauze/sponge, Internal |
| Applicant | KENTRON HEALTH CARE, INC. 4330 SHERIDAN ST. Hollywood, FL 33021 |
| Contact | Nari Sadarangani |
| Correspondent | Nari Sadarangani KENTRON HEALTH CARE, INC. 4330 SHERIDAN ST. Hollywood, FL 33021 |
| Product Code | EFQ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-21 |
| Decision Date | 1995-11-06 |
Trademark Results [KENTEX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KENTEX 74169774 1801419 Dead/Cancelled |
KENTEX ELECTRONIC CO., LTD. 1991-05-24 |
 KENTEX 73610926 1560979 Dead/Cancelled |
KENTEX INDUSTRIES, INC. 1986-07-23 |
 KENTEX 73587700 1438462 Dead/Cancelled |
KENTEX CORPORATION 1986-03-13 |
 KENTEX 73587680 1439573 Dead/Cancelled |
KENTEX CORPORATION 1986-03-13 |
 KENTEX 73101261 1077839 Dead/Cancelled |
Mardon Flexible Packaging Limited 1976-09-27 |
 KENTEX 72163589 0761902 Dead/Cancelled |
Textile Apron Company, Inc. 1963-02-27 |
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