Medical Technical Products: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Medical Technical Products” (first 1987, latest 1994), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 118 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 |
|---|---|---|---|
| HQC | Unit, Phacofragmentation | 5 | 5 |
| FRN | Pump, Infusion | 2 | 2 |
| HOC | Clip, Iris Retractor | 1 | 1 |
Review panels
- Ophthalmic (6)
- General Hospital (2)
Most recent Medical Technical Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K940083 | STANDARD PHACO TIP 15, 30, 45, 60 | HQC | 1994-09-28 | 264 |
| K940088 | MEDICAL TECHNICAL PRODUCTS STANDARD ULTRASONIC HANDPIECE | HQC | 1994-08-04 | 209 |
| K940084 | MODEL 2000 OPHTHALMIC SURGICAL SYSTEM | HQC | 1994-06-17 | 161 |
| K910335 | MTP TRANSPORT INFUSION PUMP, MODEL NO. MTPLEA | FRN | 1991-03-13 | 47 |
| K905251 | MTP TRANSPORT INFUSION PUMP MODEL NO. 1001A | FRN | 1991-02-07 | 78 |
| K904612 | I/A-PHACO SYSTEM (IRR./ASPIR./AND PHACO./SYSTEM) | HQC | 1990-12-26 | 76 |
| K871474 | PART #860070 ULTRAPAK & #860075 ULTRAPAK | HOC | 1987-08-10 | 118 |
| K871473 | PART #860065 IA PAK & PART #860060 IA PAK | HQC | 1987-08-10 | 118 |
Recalls
openFDA lists no recalls under a recalling firm named Medical Technical Products.
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 Medical Technical Products (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.
- Medical Analysis Systems, Inc. (107 510(k)s)
- Medical Components, Inc. (63 510(k)s)
- Medical Advances, Inc. (57 510(k)s)
- Medical Diagnostic Technologies, Inc. (57 510(k)s)
- Medical Devices, Inc. (49 510(k)s)
- Medical Device Technologies, Inc. (46 510(k)s)
- Medical Specialties, Inc. (40 510(k)s)
- Medical Device Inspection Co., Inc. (30 510(k)s)
- Medical Engineering Corp. (28 510(k)s)
- Medical Data Electronics (27 510(k)s)
- Medical Graphics Corp. (25 510(k)s)
- Medical Innovations Corp. (24 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Medical Technical Products?
FDA lists 8 510(k) clearances under the applicant name “Medical Technical Products” (first 1987, latest 1994), across 3 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 Medical Technical Products?
The median time from FDA receipt to decision across 510(k)s cleared under the name Medical Technical Products is 118 days.
Which FDA product codes appear under Medical Technical Products?
The most frequent FDA product codes under this applicant name are HQC (Unit, Phacofragmentation, 5); FRN (Pump, Infusion, 2); HOC (Clip, Iris Retractor, 1).
Next steps
- See all 8 Medical Technical Products clearances with predicates and recalls
- Run predicate analysis for product code HQC, Medical Technical Products'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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.