Mumtaz I. Malik: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Mumtaz I. Malik” (first 1988, latest 1990), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 179 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 |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | 4 | 4 |
| EFQ | Gauze/Sponge, Internal | 1 | 1 |
| GEN | Forceps, General & Plastic Surgery | 1 | 1 |
| LRP | Tray, Surgical | 1 | 1 |
Review panels
Most recent Mumtaz I. Malik 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K901521 | OSTEOTOMES OF VARIOUS TYPES | LXH | 1990-09-28 | 179 |
| K901511 | CHISEL, BONE, SURGICAL | LXH | 1990-09-28 | 183 |
| K901420 | VOLKMAN BONE CURRETTE 5, 5-3/4, 6-3/4, 8 | LXH | 1990-09-28 | 186 |
| K901289 | RONGEUR, ORTHOPEDIC SURGICAL INSTRUMENTS | LXH | 1990-09-28 | 192 |
| K893902 | 4 X 4 STERILE GAUZE SPONGE TRAY | EFQ | 1989-07-14 | 45 |
| K890071 | STERILE LACERATION TRAY | LRP | 1989-01-24 | 15 |
| K884195 | GENERAL SURGICAL INSTRUMENTS (VARIOUS TYPES) | GEN | 1988-10-24 | 18 |
Recalls
openFDA lists no recalls under a recalling firm named Mumtaz I. Malik.
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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Mumtaz I. Malik?
FDA lists 7 510(k) clearances under the applicant name “Mumtaz I. Malik” (first 1988, latest 1990), across 4 product codes in 2 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 Mumtaz I. Malik?
The median time from FDA receipt to decision across 510(k)s cleared under the name Mumtaz I. Malik is 179 days.
Which FDA product codes appear under Mumtaz I. Malik?
The most frequent FDA product codes under this applicant name are LXH (Orthopedic Manual Surgical Instrument, 4); EFQ (Gauze/Sponge, Internal, 1); GEN (Forceps, General & Plastic Surgery, 1).
Next steps
- See all 7 Mumtaz I. Malik clearances with predicates and recalls
- Run predicate analysis for product code LXH, Mumtaz I. Malik'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.