Identity
- Trade Name
- Geminus FDA UDI
- Generic Name
- Surgical screwdriver, single-use FDA UDI
- Model / Reference
- Driver, Peg FDA UDI
Identifiers
- Catalog Number
- DRVR-S20 FDA UDI
- Primary DI / UDI-DI
- 00841506109152 FDA UDI
- 510(k) Number
- K200538 FDA UDI
- FDA Product Code
- HRS FDA UDI
- GMDN Term
- Surgical screwdriver, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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
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: Surgical screwdriver, single-use
Geminus by Skeletal Dynamics L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical screwdriver, single-use.
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Cleared under the same submission
K200538 also covers:
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
- Forearm Plating System — SKELETAL DYNAMICS L.L.C.
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
- Skeletal Dynamics L.l.c.
Sources (1)
- FDA UDI 416ae7e0-5194-40f1-b1bd-c266a7006221 35 fields · synced May 30, 2026