Identity
- Trade Name
- TriFit TS Blade Stem FDA UDI
- Generic Name
- Orthopaedic osteotome FDA UDI
- Device Name
- DAA Box Osteotome FDA UDI
- Model / Reference
- 3999322 FDA UDI
- Description
- DAA Box Osteotome FDA UDI
Identifiers
- Catalog Number
- 3999322 FDA UDI
- Primary DI / UDI-DI
- 05055343897652 FDA UDI
- 510(k) Number
- K121563 FDA UDI
- FDA Product Code
- KWL FDA UDIKWY FDA UDIMEH FDA UDILZO FDA UDI
- GMDN Term
- Orthopaedic osteotome FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3360 FDA UDI888.3390 FDA UDI888.3353 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: Orthopaedic osteotome
TriFit TS Blade Stem by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic osteotome.
- Stratum Ankle — Medartis Inc. · Class I
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- gSource — GSOURCE, LLC. · Class I
- INSTRUMENT — Howmedica Osteonics Corp. · Class I
- ORTHOMED — ORTHO-MED, INC. · Class I
Cleared under the same submission
K121563 also covers:
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
- TriFit TS Blade Stem — CORIN LTD
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
- Corin Ltd
Sources (1)
- FDA UDI 7052f0f8-ecce-4edb-8d3a-2ee0c7b45a4b 36 fields · synced May 29, 2026