Identity
- Trade Name
- Integrity Orthopaedics FDA UDI
- Generic Name
- Orthopaedic inorganic implant inserter/extractor, single-use FDA UDI
- Device Name
- Tendon Seam™ Instrument Kit - 4 Anchor FDA UDI
- Model / Reference
- 901005 FDA UDI
- Description
- Tendon Seam™ Instrument Kit - 4 Anchor FDA UDI
Identifiers
- Catalog Number
- 901005 FDA UDI
- Primary DI / UDI-DI
- 00860013905972 FDA UDI
- FDA Product Code
- MBI FDA UDILXH FDA UDI
- GMDN Term
- Orthopaedic inorganic implant inserter/extractor, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
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
No
FDA UDI
Category: Tendon/ligament bone anchor, non-bioabsorbableOrthopaedic inorganic implant inserter/extractor, single-use
Integrity Orthopaedics by Integrity Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Integrity Orthopaedics, Inc.
Sources (1)
- FDA UDI da702c09-8eae-45f1-9b99-3e46a3500710 34 fields · synced Jun 1, 2026