| Primary Device ID | 00840124513037 |
| NIH Device Record Key | d7295969-1134-49dc-8957-557888b4a9c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PolyPrep |
| Version Model Number | CD-PP-3320-S |
| Catalog Number | CD-PP-3320-S |
| Company DUNS | 080307067 |
| Company Name | FUSION ORTHOPEDICS, LLC |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | true |
| 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 | 00840124513037 [Primary] |
| HWM | Osteotome |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-15 |
| Device Publish Date | 2024-10-07 |
| 00840124514195 | Push Pull |
| 00840124513037 | Osteotome Flexible 130mm x 20mm (Sterile) |
| 00840124513020 | Osteotome Flexible 130mm x 16mm (Sterile) |
| 00840124513013 | Osteotome Flexible 130mm x 12mm (Sterile) |
| 00840124513006 | Osteotome Flexible 130mm x 10mm (Sterile) |
| 00840124512993 | Osteotome Flexible 70mm x 20mm (Sterile) |
| 00840124512986 | Osteotome Flexible 70mm x 12mm (Sterile) |
| 00840124512979 | Osteotome Flexible 70mm x 10mm (Sterile) |
| 00840124512962 | Osteotome Straight 8mm (Sterile) |
| 00840124512955 | Osteotome Straight 7mm (Sterile) |
| 00840124512948 | Osteotome Straight 6mm (Sterile) |
| 00840124512931 | Osteotome Straight 5mm (Sterile) |
| 00840124512924 | Osteotome Straight 4mm (Sterile) |
| 00840124512917 | Osteotome Flexible 70mm x 8mm (Sterile) |
| 00840124512900 | Curette 6mm (Sterile) |
| 00840124512894 | Curette 5mm (Sterile) |
| 00840124512887 | Curette 4mm (Sterile) |
| 00840124512870 | Curette 3mm (Sterile) |
| 00840124512863 | Pulling Cartilage Remover 8mm (Sterile) |
| 00840124512856 | Pulling Cartilage Remover 7mm (Sterile) |
| 00840124512849 | Pulling Cartilage Remover 6mm (Sterile) |
| 00840124512832 | Pulling Cartilage Remover 5mm (Sterile) |
| 00840124512825 | Pulling Cartilage Remover 4mm (Sterile) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() POLYPREP 77911062 not registered Dead/Abandoned |
Plastic Dental Corporation 2010-01-13 |
![]() POLYPREP 75285762 2213912 Live/Registered |
HENKEL AG & CO. KGAA 1997-05-02 |
![]() POLYPREP 74275140 1783168 Dead/Cancelled |
Baker Hughes Incorporated 1992-05-13 |
![]() POLYPREP 73678897 1510960 Dead/Cancelled |
KENDALL COMPANY, THE 1987-08-17 |