Natrelle INSPIRA TRF-770
GUDID 10888628008427
Natrelle INSPIRA Silicone-Filled Breast Implants, TRF-770
Allergan, Inc.
Silicone gel-filled breast implant Silicone gel-filled breast implant Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface Silicone gel-filled breast implant, textured-surface| Primary Device ID | 10888628008427 |
| NIH Device Record Key | 4d3a1515-13e6-4982-896d-e9575ea1779e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Natrelle INSPIRA |
| Version Model Number | TRF-770 |
| Catalog Number | TRF-770 |
| Company DUNS | 144796497 |
| Company Name | Allergan, Inc. |
| Device Count | 1 |
| 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 | false |
| Serial Number | true |
| 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 |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10888628008427 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P020056
FDA Product Code
| FTR | Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-10-24 |
| Device Publish Date | 2018-02-28 |
Devices Manufactured by Allergan, Inc.
| 30840228302767 - SKINVIVE BY JUVEDERM XC 1ML SAMPLE | 2024-04-18 SKINVIVE BY JUVEDERM XC 1ML SAMPLE |
| 30840228302774 - JUVEDERM ULTRA PLUS XC 1ML SAMPLE | 2024-04-18 JUVEDERM ULTRA PLUS XC 1ML SAMPLE |
| 30840228302781 - JUVEDERM ULTRA XC 1ML SAMPLE | 2024-04-18 JUVEDERM ULTRA XC 1ML SAMPLE |
| 30840228302798 - JUVEDERM VOLBELLA XC 1ML SAMPLE | 2024-04-18 JUVEDERM VOLBELLA XC 1ML SAMPLE |
| 30840228302804 - JUVEDERM VOLBELLA XC 0.55ML SAMPLE | 2024-04-18 JUVEDERM VOLBELLA XC 0.55ML SAMPLE |
| 30840228302811 - JUVEDERM VOLLURE XC 1ML SAMPLE | 2024-04-18 JUVEDERM VOLLURE XC 1ML SAMPLE |
| 30840228302828 - JUVEDERM VOLUMA XC 1ML SAMPLE | 2024-04-18 JUVEDERM VOLUMA XC 1ML SAMPLE |
| 30840228302835 - JUVEDERM VOLUX XC 1ML SAMPLE | 2024-04-18 JUVEDERM VOLUX XC 1ML SAMPLE |
Trademark Results [Natrelle INSPIRA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NATRELLE INSPIRA 86095868 4800318 Live/Registered |
Allergan, Inc. 2013-10-18 |
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