FDA product code · Orthopedic · Class 2

LOD: Bone Cement

LOD is FDA's product code for "Bone Cement": a Class 2 device classified under 21 CFR 888.3027, reviewed by the Orthopedic panel. FDA flags it as an implant.

510(k) review time for LOD

Across 21 510(k) clearances under LOD decided from 2018-01-01 to 2026-10-06, the median was 117 days from FDA receipt to decision. Half took between 67 and 204 days, and 80% were decided within 239 days. These are past clearances, not a forecast for a new submission.

Days from FDA receipt to 510(k) decision, LOD, decisions 2018-01-01 to 2026-10-06 (n = 21)
Fastest20
25th percentile67
Median117
75th percentile204
80th percentile239
90th percentile277
Slowest630

Source: openFDA 510(k) records, snapshot of 2026-10-06 (openFDA data as of 2026-09-28). Compare 510(k) review times across all device types, see every code side by side in the Clearance Timeline Estimator, or browse the clearances themselves in PredicateScope.

LOD in the public FDA record

Records naming LOD, from openFDA (snapshot of 2026-09-15)
510(k) clearances, all years72
Device recalls34
Establishment listings253

Counts of records, not of devices or events. Adverse event reports for LOD are in MAUDEScope, as counts with the query shown: MAUDE has no denominator, so a report count is not a rate and does not show that a device caused an event.

FDA-recognized standards that cite LOD

4 FDA recognized consensus standards cite LOD, among them ASTM F983-86 (Reapproved 2018); ASTM F565-04 (Reapproved 2018); ASTM F983-24. Horizontal standards such as biocompatibility, sterilization and software standards can apply without citing the code.

  • 11-197 ASTM F983-86 (Reapproved 2018) — Standard Practice for Permanent Marking of Orthopaedic Implant Components
  • 11-199 ASTM F565-04 (Reapproved 2018) — Standard Practice for Care and Handling of Orthopedic Implants and Instruments
  • 11-424 ASTM F983-24 — Standard Practice for Permanent Marking of Orthopaedic Implant Components
  • 11-425 ASTM F565-21 — Standard Practice for Care and Handling of Orthopedic Implants and Instruments

Source: FDA Recognized Consensus Standards, snapshot of 2026-09-01. Search them all in the Consensus Standards Lookup.

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