Boat
GUDID 10871321001826
Labtician Ophthalmics, Inc
Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable Scleral buckling device, bioabsorbable| Primary Device ID | 10871321001826 |
| NIH Device Record Key | 204b5175-dae1-4368-a3c3-dc6f7defc9e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Boat |
| Version Model Number | S 3012 |
| Company DUNS | 248911026 |
| Company Name | Labtician Ophthalmics, Inc |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00871321000686 [Unit of Use] |
| GS1 | 10871321001826 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K875014
FDA Product Code
| HQJ | Implant, Absorbable, (Scleral Buckling Methods) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2021-01-28 |
| Device Publish Date | 2015-10-09 |
On-Brand Devices [Boat]
| 18713210001833 | S 3012 |
| 18713210001826 | S 3012 |
| 18713210001680 | S 2989 |
| 10871321001833 | S 3012 |
| 10871321001826 | S 3012 |
| 10871321001680 | S 2989 |
Trademark Results [Boat]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BOAT 87821754 5580285 Live/Registered |
Carton Brewing Company, LLC 2018-03-06 |
 BOAT 87190035 5353247 Live/Registered |
BEARD INTERNATIONAL SERVICES AND TECHNOLOGIES, L.L.C. 2016-09-30 |
 BOAT 85450899 4377112 Live/Registered |
Manring, Chris 2011-10-19 |
 BOAT 78187416 2850751 Live/Registered |
KALKOMEY ENTERPRISES, LLC 2002-11-21 |
 BOAT 73807671 1605175 Dead/Cancelled |
DIAMANDIS COMMUNICATIONS INC. 1989-06-19 |
 BOAT 73641013 1455138 Dead/Cancelled |
UNITED INDUSTRIES, INC. 1987-01-23 |
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