Progress Mankind Technology: FDA filings under this applicant name
FDA lists 17 510(k) clearances under the applicant name “Progress Mankind Technology” (first 1980, latest 1988), across 12 product codes in 4 review panels. Median 510(k) review time under this name: 65 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| GZL | Electrode, Depth | 3 | 3 |
| HAW | Neurological Stereotaxic Instrument | 2 | 2 |
| HAX | Tong, Skull For Traction | 2 | 2 |
| JOL | Catheter And Tip, Suction | 2 | 2 |
| CAZ | Anesthesia Conduction Kit | 1 | 1 |
| FLL | Continuous Measurement Thermometer | 1 | 1 |
| FRN | Pump, Infusion | 1 | 1 |
| GEA | Cannula, Surgical, General & Plastic Surgery | 1 | 1 |
| GXI | Probe, Radiofrequency Lesion | 1 | 1 |
| GYC | Electrode, Cortical | 1 | 1 |
Plus 2 more product codes.
Review panels
- Neurology (10)
- General Hospital (4)
- General and Plastic Surgery (2)
- Anesthesiology (1)
Most recent Progress Mankind Technology 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K883314 | PMT 3721-1 EPIDURAL KIT | CAZ | 1988-10-28 | 85 |
| K881616 | PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1 | JXG | 1988-09-09 | 150 |
| K871663 | PMT TRACTION TONGS | HAX | 1987-06-19 | 52 |
| K854157 | PMT ACCUPRESSURE INFUSION SYSTEM 3601 | FRN | 1986-02-13 | 125 |
| K845035 | ELECTRODE FOR NEUROLOGICAL SURGERY 2111 | GYC | 1985-07-30 | 215 |
| K845036 | TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 | LCJ | 1985-06-26 | 181 |
| K834047 | PMT-HALO/ORTHOPEDIC JACKET SYSTEM | HAX | 1984-02-17 | 86 |
| K831329 | PMT VAXIOM STEREOTACTIC SYS #FX001 | HAW | 1983-06-15 | 51 |
| K830530 | TEMP TRACE | FLL | 1983-04-06 | 47 |
| K812744 | LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER | HAW | 1981-12-03 | 65 |
7 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Progress Mankind Technology.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Progress Mankind Technology (a text match, not an official crosswalk):
- A4220 — Refill kit for implantable infusion pump (via FRN)
- E0786 — Implantable programmable infusion pump, replacement (excludes implantable intraspinal catheter) (via FRN)
- E0785 — Implantable intraspinal (epidural/intrathecal) catheter used with implantable infusion pump, replacement (via FRN)
Frequently asked questions
How many FDA 510(k) clearances are listed under Progress Mankind Technology?
FDA lists 17 510(k) clearances under the applicant name “Progress Mankind Technology” (first 1980, latest 1988), across 12 product codes in 4 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Progress Mankind Technology?
The median time from FDA receipt to decision across 510(k)s cleared under the name Progress Mankind Technology is 65 days.
Which FDA product codes appear under Progress Mankind Technology?
The most frequent FDA product codes under this applicant name are GZL (Electrode, Depth, 3); HAW (Neurological Stereotaxic Instrument, 2); HAX (Tong, Skull For Traction, 2).
Next steps
- See all 17 Progress Mankind Technology clearances with predicates and recalls
- Run predicate analysis for product code GZL, Progress Mankind Technology's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.