Minnesota Mining and Mfg. Co.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Minnesota Mining and Mfg. Co.” (first 1983, latest 2002), across 8 product codes in 3 review panels. Median 510(k) review time under this name: 113 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 |
|---|---|---|---|
| JOJ | Indicator, Physical/Chemical Sterilization Process | 2 | 2 |
| DQD | Stethoscope, Electronic | 1 | 1 |
| DRX | Electrode, Electrocardiograph | 1 | 1 |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) | 1 | 1 |
| EJR | Agent, Polishing, Abrasive, Oral Cavity | 1 | 1 |
| FRN | Pump, Infusion | 1 | 1 |
| FXX | Mask, Surgical | 1 | 1 |
Plus 1 more product codes.
Review panels
- General Hospital (4)
- Cardiovascular (3)
- Dental (1)
Most recent Minnesota Mining and Mfg. Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K013228 | 3M COMPLY 1248 GAS PLASMA CHEMICAL INDICATOR | JOJ | 2002-01-18 | 113 |
| K000355 | 3M COMPLY 1249 LIQUID PERACETIC ACID CHEMICAL INDICATOR | JOJ | 2000-08-23 | 201 |
| K000690 | 3M RED DOT RADIOLUCENT MONITORING ELECTRODE WITH CONDUCTIVE ADHESIVE | DRX | 2000-05-17 | 78 |
| K990482 | 3M CLINPRO PROPHY PASTE, MODEL 12611 | EJR | 1999-05-13 | 86 |
| K961848 | 3M LITTMANN ELECTRONIC STETHOSCOPE | DQD | 1997-09-26 | 501 |
| K965043 | 3M 1830 FLUID BLOCK ANTI-FOG TIE-ON SURGICAL MASK AND 3M 1830FS FLUID BLOCK ANTI-FOG TIE-ON SURGICAL MASK WITH FACE SHIE | FXX | 1997-03-10 | 83 |
| K954900 | 3M RED DOT ECG LEAD WIRES A | DSA | 1996-07-15 | 264 |
| K940446 | 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) | FRN | 1994-08-15 | 195 |
| K837117 | 3M FERLIC CHEST FILTER, X-RAY COMPENSATING FILTER | — | 1983-03-09 | 35 |
Recalls
openFDA lists no recalls under a recalling firm named Minnesota Mining and Mfg. Co..
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 Minnesota Mining and Mfg. Co. (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)
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Minnesota Laser Corp. (12 510(k)s)
- Minnesota Scientific, Inc. (5 510(k)s)
- Minnesota Valley Engineering, Inc. (4 510(k)s)
- Minnesota Medical Development, Inc. (3 510(k)s)
- Minnesota Prophy Power, Inc. (2 510(k)s)
- Minnesota Medical Technologies (1 510(k)s)
- Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Minnesota Mining and Mfg. Co.?
FDA lists 9 510(k) clearances under the applicant name “Minnesota Mining and Mfg. Co.” (first 1983, latest 2002), across 8 product codes in 3 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 Minnesota Mining and Mfg. Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Minnesota Mining and Mfg. Co. is 113 days.
Which FDA product codes appear under Minnesota Mining and Mfg. Co.?
The most frequent FDA product codes under this applicant name are JOJ (Indicator, Physical/Chemical Sterilization Process, 2); DQD (Stethoscope, Electronic, 1); DRX (Electrode, Electrocardiograph, 1).
Next steps
- See all 9 Minnesota Mining and Mfg. Co. clearances with predicates and recalls
- Run predicate analysis for product code JOJ, Minnesota Mining and Mfg. Co.'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.