BIO-VENT
Implant, Endosseous, Root-form
CORE-VENT CORP.
The following data is part of a premarket notification filed by Core-vent Corp. with the FDA for Bio-vent.
Pre-market Notification Details
| Device ID | K883717 |
| 510k Number | K883717 |
| Device Name: | BIO-VENT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | CORE-VENT CORP. 15821 VENTURA BLVD. Encino, CA 91436 |
| Contact | Niznick, Dmd |
| Correspondent | Niznick, Dmd CORE-VENT CORP. 15821 VENTURA BLVD. Encino, CA 91436 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-30 |
| Decision Date | 1989-09-01 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024019126 | K883717 | 000 |
| 00889024019089 | K883717 | 000 |
| 00889024019072 | K883717 | 000 |
| 00889024019065 | K883717 | 000 |
Trademark Results [BIO-VENT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIO-VENT 74065434 1655481 Dead/Cancelled |
CORE-VENT CORPORATION 1990-06-04 |
 BIO-VENT 72434602 0985761 Dead/Expired |
HANCOR, INC. 1972-09-05 |
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