Identity
- Trade Name
- RELIEVA SPINPLUS FDA UDI
- Generic Name
- Nasal haemostatic balloon FDA UDI
- Device Name
- RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT FDA UDI
- Model / Reference
- RSP0516 FDA UDI
- Description
- RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT FDA UDI
Identifiers
- Catalog Number
- RSP0516 FDA UDI
- Primary DI / UDI-DI
- 10705031233034 FDA UDI
- 510(k) Number
- K143541 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- Nasal haemostatic balloon FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Nasal haemostatic balloon
Relieva Spinplus by Acclarent, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Nasal haemostatic balloon.
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Cleared under the same submission
K143541 also covers:
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
- RELIEVA SPINPLUS — ACCLARENT, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Acclarent, Inc.
Sources (1)
- FDA UDI 5b0cd4cf-618e-487a-a026-203fc9d094dd 37 fields · synced Jun 8, 2026