Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
Progress Mankind Technology — Predicate Candidate Screening
17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
65 daysmedian FDA review time
181 days90th percentile
17clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K883314 | PMT 3721-1 EPIDURAL KIT | Progress Mankind Technology | 1988-10-28 | 85 | 0 |
| K881616 | PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1 | Progress Mankind Technology | 1988-09-09 | 150 | 0 |
| K871663 | PMT TRACTION TONGS | Progress Mankind Technology | 1987-06-19 | 52 | 0 |
| K854157 | PMT ACCUPRESSURE INFUSION SYSTEM 3601 | Progress Mankind Technology | 1986-02-13 | 125 | 0 |
| K845035 | ELECTRODE FOR NEUROLOGICAL SURGERY 2111 | Progress Mankind Technology | 1985-07-30 | 215 | 0 |
| K845036 | TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 | Progress Mankind Technology | 1985-06-26 | 181 | 0 |
| K834047 | PMT-HALO/ORTHOPEDIC JACKET SYSTEM | Progress Mankind Technology | 1984-02-17 | 86 | 0 |
| K831329 | PMT VAXIOM STEREOTACTIC SYS #FX001 | Progress Mankind Technology | 1983-06-15 | 51 | 0 |
| K830530 | TEMP TRACE | Progress Mankind Technology | 1983-04-06 | 47 | 0 |
| K812744 | LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER | Progress Mankind Technology | 1981-12-03 | 65 | 0 |
| K810627 | MODEL 1301 BIOTAC (TM) | Progress Mankind Technology | 1981-04-02 | 24 | 0 |
| K802249 | MICROLET FAMILY OF NEEDLE/DEPTH ELECT- | Progress Mankind Technology | 1980-11-19 | 64 | 0 |
| K802152 | PMT DEPTHALON DEPTH #2102 | Progress Mankind Technology | 1980-11-19 | 72 | 0 |
| K802151 | PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC | Progress Mankind Technology | 1980-11-19 | 72 | 0 |
| K802243 | VAXIOM FAMILY OF RF LESION PROBES & ELEC | Progress Mankind Technology | 1980-11-12 | 57 | 0 |
| K801134 | MICROVAC | Progress Mankind Technology | 1980-05-30 | 18 | 0 |
| K801127 | MACROVAC | Progress Mankind Technology | 1980-05-30 | 18 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda