Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in TaiwanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list United Orthopedic Corporation with 61 510(k) clearances and 12 device recalls. The most recent is a 510(k) clearance dated Sep 2, 2026: Momentum Acetabular Cup System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 2, 2026 | Momentum Acetabular Cup SystemK253948 · LZO | 510(k) clearances |
| Sep 25, 2025 | Stem Extension Line (U2 Total Knee System—PSA Type)K252725 · JWH | 510(k) clearances |
| Aug 22, 2025 | Stem Extension Line (USTAR II System)K252303 · KRO | 510(k) clearances |
| Jul 31, 2025 | U2 Total Knee System – PF+ Patella; USTAR II System– PF+ PatellaK243656 · MBH | 510(k) clearances |
| May 1, 2025 | Resolve Modular Revision Hip StemK242315 · MEH | 510(k) clearances |
| Jan 6, 2025 | Conformity Stem Extension Line, #0K243466 · LZO | 510(k) clearances |
| Dec 20, 2024 | Cellbrick Knee SpacerK243024 · JWH | 510(k) clearances |
| Aug 30, 2024 | Conformity Stem Extension LineK242249 · LZO | 510(k) clearances |
| Jan 3, 2024 | USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 Class II · Their is a potential that the implant curved stem may be oriented incorrectly. | Device recalls |
| Jan 3, 2024 | USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213Class II · Their is a potential that the implant curved stem may be oriented incorrectly. | Device recalls |
| Jan 3, 2024 | USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9Class II · Their is a potential that the implant curved stem may be oriented incorrectly. | Device recalls |
| Nov 24, 2017 | U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Knee system is indicateClass II · UOC received a customer compliant report from our distributor on October 31, 2017 which stated that contents of the pac | Device recalls |
| Nov 24, 2017 | U2 Total Knee System Tibial Insert, PSA, #1, 21mm Thick Catalogue number 2303-5016 The U2 Total Knee system is indicated in knee arthroplClass II · UOC received a customer compliant report from our distributor on October 31, 2017 which stated that contents of the pac | Device recalls |
| Feb 10, 2017 | UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral coClass II · The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during sur | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
