| Primary Device ID | 00190707000479 |
| NIH Device Record Key | b927136f-24b5-4166-a334-de36035422dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Safety Force |
| Version Model Number | 3804-441 |
| Company DUNS | 062165188 |
| Company Name | ORTHO ORGANIZERS, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00190707000479 [Primary] |
| DZB | Headgear, extraoral, orthodontic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-03-14 |
| Device Publish Date | 2016-09-24 |
| 00190707000493 | SAFETY FORCE MODULES HEAVY BLACK |
| 00190707000486 | SAFETY FORCE MODULES HEAVY BLUE |
| 00190707000479 | SAFETY FORCE MODULES MEDIUM BLACK |
| 00190707000462 | SAFETY FORCE MODULES MEDIUM BLUE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SAFETY FORCE 97616743 not registered Live/Pending |
Plymouth Rock Management Company of NewJersey 2022-10-03 |
![]() SAFETY FORCE 97616735 not registered Live/Pending |
Plymouth Rock Management Company of NewJersey 2022-10-03 |