Is this your brand? Sign in to claim ownership.
Sign in to claim this brandACUITIVE TECHNOLOGIES
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 50 Commerce Drive, Allendale, NJ, 07401
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014560508
- DUNS Number
- —
Catalogue (129)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 5 x10mm CitreLock Xpress Implant Kit | 70-812-0510 | FDA UDI | Class II | Active |
| Citrefix 2.9mm Inserter | 40-100-4029 | FDA UDI | Class I | Active |
| Citrefix Plunger Safety Clip | 40-100-0005 | FDA UDI | Class I | Active |
| 5.5 X 24mm Citrefix Implant | 30-110-7055 | FDA UDI | Class II | Active |
| 5 x 10mm CitreLock Implant | 30-102-0510 | FDA UDI | Class II | Active |
| Citrefix 3.5mm Drill | 40-100-5035 | FDA UDI | Class I | Active |
| Citrefix 2.9mm Drill | 40-100-5029 | FDA UDI | Class I | Active |
| Citrelock ACL 9mm Femoral Reamer | 40-103-3090 | FDA UDI | Class I | Active |
| 5 x 15mm CitreLock Implant | 30-102-0515 | FDA UDI | Class II | Active |
| Citrelock ACL 8mm Dilator | 40-103-2080 | FDA UDI | Class I | Active |
| Citrefix 4.5mm Inserter | 40-100-4045 | FDA UDI | Class I | Active |
| CitreLock Inserter Small | 40-102-0001 | FDA UDI | Class I | Active |
| CitreLock 8.0mm Reamer | 40-101-1080 | FDA UDI | Class I | Active |
| Citrefix 3.5mm Inserter Center Shaft | 40-100-1035 | FDA UDI | Class I | Active |
| Citrefix Small Drill Guide | 40-100-5100 | FDA UDI | Class I | Active |
| Citrefix 3.5mm Inserter | 40-100-4035 | FDA UDI | Class I | Active |
| Citrefix 5.5mm Inserter | 40-100-4055 | FDA UDI | Class I | Active |
| 6 x 23mm CitreLock Xpress Implant Kit | 70-812-0623 | FDA UDI | Class II | Active |
| 10 x 23mm Citrelock ACL Implant | 30-103-1023 | FDA UDI | Class II | Active |
| Citrefix 5.5mm Inserter Center Shaft | 40-100-1055 | FDA UDI | Class I | Active |
| Citrefix Large Drill Guide | 40-100-5101 | FDA UDI | Class I | Active |
| CitreLock Tendon Fixation Tray | 40-898-0003 | FDA UDI | Class I | Active |
| Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL | K220833 | FDA 510(k) | Class II | Active |
| Citregen Tendon Interference Screw and Citrelock | K200725 | FDA 510(k) | Class II | Active |
| Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants | K221468 | FDA 510(k) | Class II | Active |
| The Citrefix Knotless Suture Anchor | K203334 | FDA 510(k) | Class II | Active |
| Citrepore™ | K240450 | FDA 510(k) | Class II | Active |
| Citrelock® Duo | K232592 | FDA 510(k) | Class II | Active |
| CITRESPLINE and CITRELOCK ACL Implants | K210239 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.