Identity
- Trade Name
- Head Release with Silicone Handle FDA UDI
- Generic Name
- Orthopaedic instrument extractor FDA UDI
- Model / Reference
- 88036 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290115935127 FDA UDI
- FDA Product Code
- NKB FDA UDIMNI FDA UDIMNH FDA UDI
- GMDN Term
- Orthopaedic instrument extractor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 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 instrument extractor
Head Release with Silicone Handle by Premia Spine Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic instrument extractor.
- Novation — Exactech, Inc. · Class II
- Truliant — Exactech, Inc. · Class I
- Specials — SeaSpine Orthopedics Corporation · Class I
- ORTHOMED — ORTHO-MED, INC. · Class I
- Equinoxe — Exactech, Inc. · Class II
- Invictus — ALPHATEC SPINE, INC. · Class I
- Envoy Percutaneous Implant Guide System — SPINEOLOGY INC. · Class I
- 5.0 X 60MM OUTER SLEEVE — OsteoCentric Technologies,Inc · Class I
Cleared under the same submission
K150380 also covers:
- Cannulated Screwdriver — PREMIA SPINE LTD
- Cannulated Screwdriver short — PREMIA SPINE LTD
- Cannulated Tap Ø 6.5 mm — PREMIA SPINE LTD
- Compressor — PREMIA SPINE LTD
- Distractor — PREMIA SPINE LTD
- Distractor for Open Procedure — PREMIA SPINE LTD
- Fix connector power drill adaptor — PREMIA SPINE LTD
- Head Releaser — PREMIA SPINE LTD
- Inner Dilator — PREMIA SPINE LTD
- K-Wire, Blunt Beveled Tip, L=335, Ø 1.7 mm KWA — PREMIA SPINE LTD
- MIS Cannulated Pedicle Probe — PREMIA SPINE LTD
- MIS Compressor — PREMIA SPINE LTD
K170061 also covers:
- Cannulated Screwdriver — PREMIA SPINE LTD
- Cannulated Screwdriver short — PREMIA SPINE LTD
- Cannulated Tap Ø 6.5 mm — PREMIA SPINE LTD
- Compressor — PREMIA SPINE LTD
- Distractor — PREMIA SPINE LTD
- Distractor for Open Procedure — PREMIA SPINE LTD
- Fix connector power drill adaptor — PREMIA SPINE LTD
- Head Releaser — PREMIA SPINE LTD
- Inner Dilator — PREMIA SPINE LTD
- K-Wire, Blunt Beveled Tip, L=335, Ø 1.7 mm KWA — PREMIA SPINE LTD
- K-Wire, Blunt Blunt Tip, L=600, Ø1.7mm P.Drill — PREMIA SPINE LTD
- K-Wire, Blunt Sharp Tip, L=335, Ø1.7mm KWA — PREMIA SPINE LTD
K231844 also covers:
- Cannulated Screwdriver — PREMIA SPINE LTD
- Cannulated Screwdriver short — PREMIA SPINE LTD
- Cannulated Tap Ø 6.5 mm — PREMIA SPINE LTD
- Cannulated Tapered Pedicle Screw — PREMIA SPINE LTD
- Cannulated Tapered Pedicle Screw — PREMIA SPINE LTD
- Cannulated Tapered Pedicle Screw — PREMIA SPINE LTD
- Cannulated Tapered Pedicle Screw — PREMIA SPINE LTD
- Cannulated Tapered Pedicle Screw — PREMIA SPINE LTD
- Compressor — PREMIA SPINE LTD
- Distractor — PREMIA SPINE LTD
- Distractor for Open Procedure — PREMIA SPINE LTD
- Fix connector power drill adaptor — PREMIA SPINE 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
- Premia Spine Ltd
Sources (1)
- FDA UDI b60541d0-c5b0-45da-9ad6-8a6961562a4e 33 fields · synced Jun 6, 2026