Conphar, Inc.: FDA clearances and approvals
Conphar, Inc. has 122 FDA 510(k) clearances (first 1979, latest 1982), across 46 product codes in 12 review panels. Median 510(k) review time: 24 days.
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 |
|---|---|---|---|
| FZT | Cutter, Surgical | 21 | 21 |
| GEN | Forceps, General & Plastic Surgery | 14 | 14 |
| DXQ | Blood Pressure Cuff | 6 | 6 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 6 | 6 |
| EGN | Scissors, Surgical Tissue, Dental | 5 | 5 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 5 | 5 |
| KOD | Catheter, Urological | 5 | 5 |
| IQI | Orthosis, Limb Brace | 4 | 4 |
| EFL | Forceps, Dressing, Dental | 3 | 3 |
| GDF | Guide, Needle, Surgical | 3 | 3 |
Plus 36 more product codes.
Review panels
- General and Plastic Surgery (47)
- Gastroenterology and Urology (16)
- Cardiovascular (15)
- Physical Medicine (10)
- Dental (9)
- General Hospital (7)
- Anesthesiology (4)
- Ear, Nose and Throat (3)
- Neurology (3)
- Obstetrics and Gynecology (3)
- Ophthalmic (3)
- Orthopedic (1)
Most recent Conphar, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K821825 | CONPHAR SILICONE FEEDING TUBE | KNT | 1982-08-10 | 49 |
| K821354 | CONPHAR MAYO HEGAR NEEDLE HOLDER | GDF | 1982-06-03 | 29 |
| K821295 | OLSEN HEGAR NEEDLE HOLDERS | GDF | 1982-06-03 | 30 |
| K821289 | MAYO-HEGAR NEEDLE HOLDER | GDF | 1982-06-03 | 30 |
| K821298 | BACKHAUS CLAMP, 3 1/2 | HTD | 1982-05-28 | 24 |
| K821294 | TONSIL SCISSORS STRAIGHT 5 1/2 | EGN | 1982-05-28 | 24 |
| K821293 | BACKHAUS CLAMP, 5 1/4 | HTD | 1982-05-28 | 24 |
| K821292 | TONSIL SCISSORS 7 | EGN | 1982-05-28 | 24 |
| K821290 | LITTAUER SCISSORS 5 1/2 | HNF | 1982-05-28 | 24 |
| K821286 | IRIS SCISSORS STRAIGHT 4 1/2 | HNF | 1982-05-28 | 24 |
112 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Conphar, Inc..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Conphar, Inc. have?
Conphar, Inc. has 122 FDA 510(k) clearances (first 1979, latest 1982), across 46 product codes in 12 review panels.
How long does FDA take to clear Conphar, Inc.'s 510(k)s?
The median time from FDA receipt to decision across Conphar, Inc.'s cleared 510(k)s is 24 days.
What devices does Conphar, Inc. make?
Its most frequent FDA product codes are FZT (Cutter, Surgical, 21); GEN (Forceps, General & Plastic Surgery, 14); DXQ (Blood Pressure Cuff, 6).
Has Conphar, Inc. had device recalls?
openFDA lists no recalls under a recalling firm name matching Conphar, Inc. Related entities may recall under other names.
Next steps
- See all 122 Conphar, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FZT, Conphar, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.