Identity
- Trade Name
- Shoreline ACS FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- No Profile DTS Guide Inserter FDA UDI
- Model / Reference
- 86-1000 FDA UDI
- Description
- No Profile DTS Guide Inserter FDA UDI
Identifiers
- Catalog Number
- 86-1000 FDA UDI
- Primary DI / UDI-DI
- 10889981127411 FDA UDI
- 510(k) Number
- K161081 FDA UDI
- FDA Product Code
- OVE FDA UDI
- GMDN Term
- Spinal implant trial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Spinal implant trial
Shoreline ACS by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K161081 also covers:
- Shoreline — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
- Shoreline ACS — SeaSpine Orthopedics Corporation
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- SeaSpine Orthopedics Corporation
Sources (1)
- FDA UDI 2bcc6c08-f0db-43c3-8489-1b27e1c50218 36 fields · synced Jun 8, 2026