| Primary Device ID | 00049696869737 |
| NIH Device Record Key | a7fb8deb-3b83-4048-be3f-fbc32b92d009 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | 64431321 |
| Company DUNS | 656091279 |
| Company Name | FOURSTAR GROUP INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00049696869737 [Primary] |
| OMW | Adhesive Backed Thermal Skin Patches |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-02-13 |
| Device Publish Date | 2023-02-05 |
| 00049696561235 - B-PURE | 2025-04-07 SILICONE SCALP MASSAGER |
| 00049696561587 - B-PURE | 2025-04-07 VIBRATING UNDER EYE MASSAGER |
| 00049696122160 - Thera Plus | 2024-12-13 MP THERAPLUS FIRST AID KIT |
| 00049696712675 - VeriQuick | 2024-12-13 At Home Marijuana Drug Test |
| 00049696719018 - VeriQuick | 2024-12-13 Pregnancy Test |
| 00049696714297 - B-PURE | 2024-09-16 STAINLESS STEEL GUA SHA |
| 00049696714303 - B-PURE | 2024-09-16 JADE ROLLER |
| 00049696715973 - B-PURE | 2024-09-16 VIBRATING JADE ROLLER |