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Q Interbody Instruments 8020-90008

by VB Spine LLC United States GUDID

Product code OLO

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10888857579774 UDI-DIDate3 Mar 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Q Interbody Instruments
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable
Model / Ref / Catalog
8020-90008
Primary DI / UDI-DI
10888857579774
510(k) Number
FDA Product Code
OLO
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable
Device Class
Class II
Regulation Number
882.4560
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Width — 9 Millimeter

Other devices from VB Spine LLC

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Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Lot / Batch Number
Other properties (12)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI 3f5d85b1-8927-49c1-85bb-c95cb4f58a9a 37 fields · synced 23 Oct 2026