| Primary Device ID | 00816728021094 | 
| NIH Device Record Key | b5708275-2dfc-4323-aadf-f0721fe4226a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | PhotonBlade™ | 
| Version Model Number | PB1 | 
| Catalog Number | PB1 | 
| Company DUNS | 175697908 | 
| Company Name | INVUITY, INC. | 
| Device Count | 1 | 
| DM Exempt | false | 
| 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 | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 8667117768 | 
| customerservice@invuity.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00816728021094 [Primary] | 
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2020-04-24 | 
| Device Publish Date | 2019-06-03 | 
| 00816728020158 | he PhotonBlade is an RF device coupled with illumination that is indicated for cutting and coagu | 
| 00816728021094 | he PhotonBlade is an RF device coupled with illumination that is indicated for cutting and coagu | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  PHOTONBLADE  87017629  5210744 Live/Registered | INVUITY, INC. 2016-04-28 |